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FDA 510(k)

Arthrex Knee FiberTak® Button Suture Anchor

K-Number: K232973 · 2023-11-15

ApplicantArthrex, Inc.
Decision Date2023-11-15
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Knee FiberTak® Button Suture Anchor is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2023-11-15 under approval number K232973. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Knee FiberTak® Button Suture Anchor?

Arthrex Knee FiberTak® Button Suture Anchor is a medical device that received FDA 510(k) clearance on 2023-11-15. It is manufactured by Arthrex, Inc.. The 510(k) number is K232973.

When was Arthrex Knee FiberTak® Button Suture Anchor approved by the FDA?

Arthrex Knee FiberTak® Button Suture Anchor received FDA 510(k) clearance on 2023-11-15, under approval number K232973.

What company makes Arthrex Knee FiberTak® Button Suture Anchor?

Arthrex Knee FiberTak® Button Suture Anchor is manufactured by Arthrex, Inc..

What is the FDA product code for Arthrex Knee FiberTak® Button Suture Anchor?

The FDA product code for Arthrex Knee FiberTak® Button Suture Anchor is MBI.

Related Clinical Trials

NCT06829667 Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle Instability COMPLETED NCT05753891 Trapeziectomy: Internal Brace vs. Ligament Reconstruction (Prospective) TERMINATED

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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Related Devices (Code: MBI)

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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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