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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