FDA 510(k) Applications Submitted by Responsive Arthroscopy LLC

FDA 510(k) Number Submission Date Device Name Applicant
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
K202153 08/03/2020 Responsive Arthroscopy Suture Anchor System Responsive Arthroscopy LLC
K230094 01/12/2023 Responsive Arthroscopy Stealth and Mini Stealth All-Suture Anchors Responsive Arthroscopy LLC
K222763 09/13/2022 Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors Responsive Arthroscopy LLC


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