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Responsive Arthroscopy Wedge Push-In Suture Anchors

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190446
510(k) Type
Special
Applicant
Responsive Arthroscopy, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2019
Days to Decision
30 days
Submission Type
Summary

Responsive Arthroscopy Wedge Push-In Suture Anchors

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190446
510(k) Type
Special
Applicant
Responsive Arthroscopy, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2019
Days to Decision
30 days
Submission Type
Summary