Responsive Arthroscopy, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Responsive Arthroscopy, LLC - FDA 510(k) Cleared Devices
Recent clearances: Mini Superhawk Suture Anchor System, Shadow Knotless All-Suture Anchors, Responsive Arthroscopy Stealth and Mini Stealth All-Suture Anchors
11
Total
11
Cleared
0
Denied
Responsive Arthroscopy, LLC has 11 FDA 510(k) cleared orthopedic devices. Based in Minneapolis, US.
Latest FDA clearance: Oct 2025. Active since 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Cor Medical Ventures, LLC, Cor Medical Ventures and Cor Medical Ventures, Inc..
FDA 510(k) Regulatory Record - Responsive Arthroscopy, LLC
11 devices
Cleared
Oct 14, 2025
Mini Superhawk Suture Anchor System
Orthopedic
25d
Cleared
Oct 23, 2023
Shadow Knotless All-Suture Anchors
Orthopedic
25d
Cleared
Aug 25, 2023
Responsive Arthroscopy Stealth and Mini Stealth All-Suture Anchors
Orthopedic
225d
Cleared
Oct 13, 2022
Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors
Orthopedic
30d
Cleared
Apr 27, 2021
Responsive Arthroscopy Thunderbolt System
Orthopedic
193d
Cleared
Sep 23, 2020
Responsive Arthroscopy Interference Screw System
Orthopedic
19d
Cleared
Sep 09, 2020
Responsive Arthroscopy Suture Anchor System
Orthopedic
37d
Cleared
Mar 27, 2019
Responsive Arthroscopy Wedge Push-In Suture Anchors
Orthopedic
30d
Cleared
Jan 18, 2019
Responsive Arthroscopy Wedge Push-In Suture Anchors
Orthopedic
269d
Cleared
Jan 03, 2019
Responsive Arthroscopy Suture Anchor System
Orthopedic
267d
Cleared
Nov 23, 2018
Responsive Arthroscopy Interference Screw System
Orthopedic
263d