Last synced on 14 November 2025 at 11:06 pm

Osprey Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K243726
510(k) Type
Traditional
Applicant
Responsive Arthroscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2025
Days to Decision
58 days
Submission Type
Summary

Osprey Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K243726
510(k) Type
Traditional
Applicant
Responsive Arthroscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2025
Days to Decision
58 days
Submission Type
Summary