Last synced on 14 November 2025 at 11:06 pm

Arthrex SwiveLock Anchor

Page Type
Cleared 510(K)
510(k) Number
K201749
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2020
Days to Decision
56 days
Submission Type
Summary

Arthrex SwiveLock Anchor

Page Type
Cleared 510(K)
510(k) Number
K201749
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2020
Days to Decision
56 days
Submission Type
Summary