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Responsive Arthroscopy Interference Screw System

Page Type
Cleared 510(K)
510(k) Number
K180573
510(k) Type
Traditional
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2018
Days to Decision
263 days
Submission Type
Summary

Responsive Arthroscopy Interference Screw System

Page Type
Cleared 510(K)
510(k) Number
K180573
510(k) Type
Traditional
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2018
Days to Decision
263 days
Submission Type
Summary