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Responsive Arthroscopy Interference Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202569
510(k) Type
Special
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2020
Days to Decision
19 days
Submission Type
Summary

Responsive Arthroscopy Interference Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202569
510(k) Type
Special
Applicant
Responsive Arthroscopy LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2020
Days to Decision
19 days
Submission Type
Summary