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FDA 510(k) Applications Submitted by Doug Kohrs
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150496
02/25/2015
Total Knee Arthroplasty System
Responsive Orthopedics LLC
K180573
03/05/2018
Responsive Arthroscopy Interference Screw System
Responsive Arthroscopy LLC
K180951
04/11/2018
Responsive Arthroscopy Suture Anchor System
Responsive Arthroscopy LLC
K181076
04/24/2018
Responsive Arthroscopy Wedge Push-In Suture Anchors
Responsive Arthroscopy LLC
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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