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The Citrefix Knotless Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K203334
510(k) Type
Traditional
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2021
Days to Decision
85 days
Submission Type
Summary

The Citrefix Knotless Suture Anchor

Page Type
Cleared 510(K)
510(k) Number
K203334
510(k) Type
Traditional
Applicant
Acuitive Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2021
Days to Decision
85 days
Submission Type
Summary