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Billing Codes

HCPCS Code C1713: Anchor/screw for opposing bone-to-bone or soft tissue-to-bone implantable

Avatar photo Katy Piper
Last Updated: August 28, 2026
Key takeaways

Key takeaways

HCPCS Code C1713 describes an anchor or screw used for opposing bone-to-bone or soft tissue-to-bone fixation in implantable procedures.

C1713 is a Level II HCPCS supply code billed by ASCs and outpatient hospitals, never by physician offices or inpatient facilities.

Missing a modifier, billing the wrong units, or confusing C1713 with a CPT code are the most common causes of denial.

Practice management software like Pabau embeds HCPCS reference data into the billing workflow, helping practices catch C1713 coding errors early.

HCPCS Code C1713 is a Level II HCPCS supply code for an anchor or screw used in opposing bone-to-bone or soft tissue-to-bone fixation. It describes the implant device, not the surgical technique, and is billed alongside a CPT procedure code in ASC and outpatient hospital settings.

The most common denial driver is billing staff treating C1713 like a CPT code. Watch for wrong units, missing modifiers, or documentation that doesn’t name the device implanted. This guide covers the code definition, clinical uses, billing rules by setting, 2026 Medicare rates, coverage criteria, common errors, and related crosswalk codes.

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HCPCS Code C1713: Definition and code details

HCPCS Code C1713 is a Level II HCPCS supply code maintained by the Centers for Medicare and Medicaid Services (CMS). The official description reads: Anchor/screw for opposing bone-to-bone or soft tissue-to-bone implantable. Unlike CPT codes, which describe the procedure performed, C1713 describes the physical device used during that procedure.

Field Detail
Code C1713
Code set HCPCS Level II (C-series)
Official description Anchor/screw for opposing bone-to-bone or soft tissue-to-bone implantable
Code type Supply/device code (not a procedure code)
Billing settings ASC and outpatient hospital (HOPD)
Maintained by CMS (Centers for Medicare and Medicaid Services)
Updated Annually by CMS

Clinical applications: Where C1713 is used

C1713 covers two mechanically distinct fixation scenarios that share one code. Understanding which scenario applies helps coders choose the right device and confirm the procedure documentation supports the claim.

Bone-to-bone fixation involves an anchor or screw used to secure two opposing bone structures. This appears most often in spinal fusion procedures and orthopedic joint reconstruction. Soft tissue-to-bone fixation involves attaching tendon, ligament, or labral tissue to bone, which is the dominant application in sports medicine surgery. The code covers both scenarios, but the operative report must clearly describe which type of fixation was performed and what device was used.

Surgical specialties that commonly bill C1713 include sports medicine and orthopedic and physical therapy practices that perform or coordinate ASC procedures. Common procedure contexts include:

  • Rotator cuff repair (tendon-to-bone fixation using soft tissue anchors)
  • Shoulder labrum repair (arthroscopic Bankart procedures)
  • ACL reconstruction with bony fixation
  • Spinal fusion procedures using pedicle screws or interbody fixation devices
  • Foot and ankle reconstruction requiring bone-to-bone fixation
  • Hip labrum repair

Confirm that the operative report names the anchor or screw device, its manufacturer, and the fixation type. A general reference to “anchor placed” is not sufficient documentation for C1713 to survive audit.

Billing settings: ASC vs outpatient hospital

C1713 is not billable in physician offices or inpatient hospital settings. It is a facility-side supply code used in ASCs and outpatient hospital departments (HOPDs). The payment mechanism, claim form, and revenue code rules all differ between these two settings.

Factor ASC (Medicare) Outpatient Hospital (HOPD)
Payment system ASC payment system OPPS (Outpatient Prospective Payment System)
Facility claim form CMS-1500 / 837P (professional) UB-04 / 837I (institutional)
Facility claim identifiers Place of service 24; Medicare has not required the SG modifier since 2008, though some payers still request it Revenue code identifies the supply line
Revenue code required No, not used on the CMS-1500 professional claim Yes, revenue code 0278 (“Other implants”)
Bundling risk Device may be packaged into procedure payment at lower ASC rates Device separately payable under OPPS when criteria met
Physician’s professional claim CMS-1500, billed separately by the surgeon under their own NPI CMS-1500, billed separately by the surgeon under their own NPI

Some commercial and Medicaid payers still require ASCs to submit facility claims on UB-04 instead of CMS-1500. Confirm the required claim form in each payer contract before billing.

ASC coders should verify current CMS payment indicator files each year. This confirms whether C1713 is separately reimbursable or packaged into the procedure’s ASC rate. CMS updates these indicators annually in the OPPS/ASC final rule.

How to bill C1713: Step-by-step guidelines

Billing C1713 correctly requires pairing the supply code with the right procedure code and supporting it with device-specific documentation. These steps apply to both ASC and outpatient hospital claims, following the guidance in standard medical billing workflows.

  1. Confirm the device and procedure. Verify with the operative report that an anchor or screw meeting the C1713 description was implanted during a covered bone-to-bone or soft tissue-to-bone fixation procedure.
  2. Identify the paired CPT code. C1713 is a supply code billed with the matching CPT code, such as CPT 29827 for rotator cuff repair or CPT 22630 for spinal fusion. The CPT code describes the procedure. C1713 describes the device.
  3. Set the correct unit count. Each unit of C1713 represents one anchor or screw. Bill three units if the operative report documents three anchors placed. Do not bill a flat “1” if the operative report documents multiple devices.
  4. Match the claim to the setting. Outpatient hospital (HOPD) claims carry revenue code 0278 (“Other implants”) on the UB-04. Medicare ASC facility claims skip the revenue code and use the CMS-1500 instead, identified by place of service 24.
  5. Attach supporting documentation. Include the device implant log identifying manufacturer name, model number, and lot number. This documentation is required for implant supply codes and is the most common missing item in C1713 audits.
  6. Apply required modifiers and confirm the claim form. Medicare has not required the SG modifier on ASC facility claims since 2008, though many commercial and Medicaid payers still do. Check laterality modifiers (RT/LT) too, and confirm which claim form each payer expects.
  7. Verify payer coverage before submission. Medicare and commercial payer rules differ, including which claim form an ASC must use. Run eligibility verification and confirm prior authorization requirements before the procedure date.

A clean claim for C1713 has consistent device documentation, units, and a paired CPT code that match the operative report before it leaves the facility.

2026 Medicare reimbursement and fee schedule for C1713

Medicare reimbursement for C1713 varies by setting and geographic locality. Rates are set annually by CMS through the OPPS/ASC final rule. Always verify current-year rates directly from CMS rather than third-party aggregator tools, as rates change each January 1. Use the CMS fee schedule search tool to confirm 2026 rates for your locality.

Factor Notes
Rate source CMS OPPS Addendum B (outpatient hospital) and ASC payment indicators file
Geographic adjustment Rates vary by locality; use CMS locality-specific files for your facility ZIP
ASC payment indicator Verify annually – device may be packaged into the procedure payment or separately payable depending on CMS indicator status
Commercial payers Rates negotiated per contract; typically reference Medicare rates with a multiplier – verify your specific contract
Rate effective date January 1, 2026 (updated via annual OPPS/ASC final rule)

For revenue cycle teams managing high-volume orthopedic or spinal ASC billing, tracking C1713 reimbursement trends is part of broader revenue cycle management. It helps identify when payer contracts under-reimburse for implant costs relative to facility acquisition price.

Medicare coverage rules for C1713

Medicare covers C1713 when the device is medically necessary for a covered surgical procedure performed in an eligible setting. Coverage is not automatic. The claim must satisfy several criteria, and medical billing compliance requires documenting each one in the patient record before the claim is submitted.

  • Medical necessity: The anchor or screw must be medically necessary for the procedure. Support this with documented diagnosis codes, imaging findings, and conservative treatment failure where applicable.
  • Covered setting: The procedure must be performed in a Medicare-approved ASC or outpatient hospital department, not an inpatient facility or physician office.
  • Covered procedure pairing: The surgical CPT code billed alongside C1713 must be a covered Medicare procedure. If the procedure itself is excluded, the device code will also deny.
  • Device documentation: The implant log must be present in the patient record. Medicare auditors routinely request device logs during post-payment reviews of implant supply codes.
  • LCD/NCD compliance: Check whether a Local Coverage Determination (LCD) or National Coverage Determination (NCD) applies to the specific procedure being coded. LCDs set procedure-specific coverage criteria that vary by Medicare Administrative Contractor (MAC) region.

When in doubt about Medicare coverage for a C1713 application, consult the CMS LCD database at CMS.gov. Contacting your MAC directly before the procedure also works.

Pro Tip

Pull your C1713 denial rate by payer quarterly. If one payer consistently denies on medical necessity while others approve the same procedure, the cause is likely missing LCD documentation for that MAC region. Fix the documentation template, not the code.

Common billing errors with C1713 and how to avoid them

C1713 denial patterns are predictable. Most errors fall into one of five categories, and each one has a straightforward prevention measure. Understanding these through proper denial management strategies reduces write-offs on high-cost implant claims.

  • Confusing C1713 with a CPT code. C1713 is a HCPCS supply code, not a CPT procedure code. Billing it as a standalone claim without a paired CPT procedure code will deny. The CPT code describes what the surgeon did. C1713 describes the device used.
  • Incorrect unit count. Each anchor or screw is one unit. Billing “1 unit” when three anchors were placed leaves revenue on the table. Billing more units than documented in the operative report triggers fraud flags. Match units to the implant log exactly.
  • Missing or incomplete device documentation. A chargemaster line item for “anchor” is not sufficient documentation. The claim must be supported by a device implant log that includes the manufacturer name, model, and lot number.
  • Wrong claim form or NPI. C1713 belongs on the facility’s own claim, not the surgeon’s professional claim. Medicare ASC claims use CMS-1500 with place of service 24. HOPD claims use UB-04 with revenue code 0278. Some commercial and Medicaid payers still require ASCs to bill on UB-04, so confirm the correct form with each payer before submitting.
  • Assuming separate payment when device is packaged. CMS bundles certain supply codes into the procedure’s composite rate under OPPS. If the CMS payment indicator for C1713 shows it is packaged for a given procedure, billing it separately will result in a denial. Check the OPPS Addendum B annually.

Several other Level II HCPCS codes cover related implant devices. Choosing the wrong code when C1713 applies (or vice versa) is a common coding error in orthopedic and spinal billing. Use the AAPC HCPCS lookup tool or the PGM Billing HCPCS search to verify current descriptions before selecting a code.

Code Description When to use instead of C1713
C1713 Anchor/screw for opposing bone-to-bone or soft tissue-to-bone implantable Standard anchor/screw fixation device in ASC/HOPD procedures
C1889 Implantable/insertable device, not otherwise classified Device does not fit any specific HCPCS implant code description – use C1889 as a true miscellaneous code, not as a default when C1713 applies
C1776 Joint device (implantable) Device replaces or augments a joint surface rather than providing fixation between tissue planes
C1762 Connective tissue, human (includes fascia lata) Biological tissue graft used in lieu of a mechanical anchor or screw device

How Pabau simplifies C1713 billing

Standalone HCPCS lookup tools like HcpcsData.com and PayerPrice show the code description and a fee-schedule estimate. They don’t connect to the billing workflow. Coders manually retype code details into a separate system, and that’s where transcription errors creep into high-cost implant claims like C1713.

Pabau claims management workflow for supply code billing
Pabau’s claims management workflow flags mismatched units and missing modifiers before a C1713 claim leaves the practice.

Practice management software like Pabau embeds claim scrubbing directly into the billing workflow, catching C1713 errors before submission. It flags mismatched units, missing modifiers, and missing device documentation at the point of entry, before a denial arrives.

Pabau automated communication and workflow tracking
Pabau’s automated workflows send follow-up reminders on outstanding documentation, so a missing implant log doesn’t stall a C1713 claim.

For high-volume implant billing, automated billing workflows cut the manual work of checking device documentation on every case. The platform’s superbill documentation captures the device detail C1713 claims need. Reporting surfaces denial patterns by code, so billing teams catch recurring errors before they compound.

For practices with multiple locations, a consistent HCPCS billing workflow reduces revenue leakage from coding variation between sites. The billing software comparison for ASC practices covers what to prioritize when evaluating platforms.

Reduce C1713 billing errors before they become denials

Pabau’s claims management software embeds HCPCS code reference and claim scrubbing directly into your billing workflow. Catch missing modifiers, incorrect units, and missing documentation at the point of entry, not after the denial arrives.

Pabau claims management dashboard

Conclusion

C1713 denials are rarely mysterious. The repeat offenders are wrong units, missing device logs, a wrong claim form, and a packaged procedure rate the biller didn’t check. Practices that recover the most on implant supply billing standardize their documentation checklist for C1713 before the claim is built. They don’t wait for the denial to arrive.

Pabau’s integrated claims management tools help orthopedic and spinal ASC billing teams catch these errors at the point of entry. To see how claim scrubbing and HCPCS workflow automation work inside the platform, book a demo with the Pabau team.

Continue your research

Continue your research

Need a framework for reducing claim denials across your practice? Denial management in healthcare covers the structured approaches billing teams use to track, appeal, and prevent recurring denials.

Want to understand how ASC billing fits into the broader billing picture? What is revenue cycle management explains how supply code billing connects to overall practice financial performance.

Looking for guidance on medical billing compliance requirements? Medical billing compliance outlines the documentation and regulatory requirements that apply to implant supply code claims.

Frequently asked questions

What does HCPCS Code C1713 cover?

HCPCS Code C1713 is a Level II HCPCS supply code. It covers an anchor or screw device used for opposing bone-to-bone or soft tissue-to-bone fixation in implantable surgical procedures. It describes the physical device, not the surgical technique, and is billed alongside a CPT procedure code in ASC and outpatient hospital settings.

How do you bill HCPCS Code C1713 correctly?

For Medicare, bill C1713 on the ASC’s CMS-1500 facility claim with place of service 24, or the HOPD’s UB-04 claim with revenue code 0278. Either way, pair it with the relevant CPT code, using one unit per anchor or screw placed to match the operative report and implant log. Include the device manufacturer, model, and lot number, and confirm with commercial or Medicaid payers whether they require UB-04 for ASC claims instead.

Is HCPCS C1713 covered by Medicare?

Yes, Medicare covers C1713 when the device is used in a medically necessary procedure performed in an approved ASC or outpatient hospital. Coverage requires documented medical necessity, a covered paired CPT procedure code, and a complete device implant log. Check your MAC’s LCD database for any procedure-specific coverage criteria.

In which settings can C1713 be billed?

C1713 is billed in ambulatory surgical centers (ASCs) and outpatient hospital departments (HOPDs) only, never in physician offices or inpatient settings. For Medicare, the ASC’s facility claim goes on a CMS-1500, while the HOPD’s facility claim goes on a UB-04. Either way, the facility bills it separately from the surgeon’s professional claim.

What are the most common billing errors with C1713?

The five most common errors include unit counts that don’t match the operative report, missing implant log documentation, and confusing C1713 with a CPT code. Two more: billing it under the surgeon’s claim instead of the facility’s, and assuming separate payment when CMS already packaged the device into the rate.

What is the difference between bone-to-bone and soft tissue-to-bone fixation for C1713?

Bone-to-bone fixation involves securing two opposing bone structures (common in spinal fusion and joint reconstruction). Soft tissue-to-bone fixation involves attaching tendon, ligament, or labral tissue to bone (common in rotator cuff repair and labrum repair). C1713 covers both fixation types under one code, but the operative report must specify which type was performed.

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