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FDA 510(k)

Osprey Suture Anchor

K-Number: K243726 · 2025-01-30

ApplicantResponsive Arthroscopy, Inc.
Decision Date2025-01-30
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Osprey Suture Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Responsive Arthroscopy, Inc.. It received FDA 510(k) clearance on 2025-01-30 under 510(k) 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. The listed applicant is Responsive Arthroscopy, Inc.. The 510(k) number is K243726.

When did Osprey Suture Anchor receive FDA 510(k) clearance?

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

Who is the listed applicant for Osprey Suture Anchor?

The FDA 510(k) record lists Responsive Arthroscopy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Osprey Suture Anchor?

The FDA product code for Osprey Suture Anchor is MBI.

Other records listing Responsive Arthroscopy, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261632Thunderbolt SystemK253010Mini Superhawk Suture Anchor SystemK233258Shadow Knotless All-Suture AnchorsK230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsK222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsK203121Responsive Arthroscopy Thunderbolt System

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Related Devices (Code: MBI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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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