FDA 510(k)

Osprey Suture Anchor

K-Number: K243726 · 2025-01-30

Decision Date2025-01-30

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Osprey Suture Anchor is a medical device manufactured by Responsive Arthroscopy, Inc.. It received FDA 510(k) clearance on 2025-01-30 under approval number K243726. 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 Osprey Suture Anchor?

Osprey Suture Anchor is a medical device that received FDA 510(k) clearance on 2025-01-30. It is manufactured by Responsive Arthroscopy, Inc.. The 510(k) number is K243726.

When was Osprey Suture Anchor approved by the FDA?

Osprey Suture Anchor received FDA 510(k) clearance on 2025-01-30, under approval number K243726.

What company makes Osprey Suture Anchor?

Osprey Suture Anchor is manufactured by Responsive Arthroscopy, Inc..

What is the FDA product code for Osprey Suture Anchor?

The FDA product code for Osprey Suture Anchor is MBI.

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

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