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Responsive Arthroscopy Suture Anchor System

Page Type
Cleared 510(K)
510(k) Number
K202153
510(k) Type
Special
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
37 days
Submission Type
Summary

Responsive Arthroscopy Suture Anchor System

Page Type
Cleared 510(K)
510(k) Number
K202153
510(k) Type
Special
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2020
Days to Decision
37 days
Submission Type
Summary