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FDA 510(k) Applications Submitted by Douglas Kohrs
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190446
02/25/2019
Responsive Arthroscopy Wedge Push-In Suture Anchors
Responsive Arthroscopy LLC
K202569
09/04/2020
Responsive Arthroscopy Interference Screw System
Responsive Arthroscopy LLC
K203121
10/16/2020
Responsive Arthroscopy Thunderbolt System
Responsive Arthroscopy LLC
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