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FDA 510(k)

CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver

K-Number: K171592 · 2017-08-29

ApplicantConmed Corporation
Decision Date2017-08-29
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2017-08-29 under approval number K171592. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver?

CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver is a medical device that received FDA 510(k) clearance on 2017-08-29. It is manufactured by Conmed Corporation. The 510(k) number is K171592.

When was CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver approved by the FDA?

CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver received FDA 510(k) clearance on 2017-08-29, under approval number K171592.

What company makes CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver?

CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver is manufactured by Conmed Corporation.

What is the FDA product code for CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver?

The FDA product code for CrossFT™ Knotless Biocomposite Suture Anchor with Disposable Driver is MAI.

Related Clinical Trials

NCT04552119 Safety of Treatment of Shoulder Repair COMPLETED NCT07491276 Efficacy of Using Knotless Barbed Suture vs N-Butyl Cyanoacrylate Glue Tissue Adhesive for Closure of Intraoral Surgical Incisions ACTIVE_NOT_RECRUITING

Related PubMed Literature

PMID: 40868376 Correlation Analysis of Suture Anchor Pull-Out Strength with Cortical Bone Thickness and Cancellous Bone Density on a Finite Element Model. Bioengineering (Basel, Switzerland) (2025)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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