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Responsive Arthroscopy, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253010Mini Superhawk Suture Anchor SystemOctober 14, 2025
K243726Osprey Suture AnchorJanuary 30, 2025
K233258Shadow Knotless All-Suture AnchorsOctober 23, 2023
K230094Responsive Arthroscopy Stealth and Mini Stealth All-Suture AnchorsAugust 25, 2023
K222763Responsive Arthroscopy Mustang and Mustang Knotless Suture AnchorsOctober 13, 2022
K203121Responsive Arthroscopy Thunderbolt SystemApril 27, 2021
K202569Responsive Arthroscopy Interference Screw SystemSeptember 23, 2020
K202153Responsive Arthroscopy Suture Anchor SystemSeptember 9, 2020
K190446Responsive Arthroscopy Wedge Push-In Suture AnchorsMarch 27, 2019
K181076Responsive Arthroscopy Wedge Push-In Suture AnchorsJanuary 18, 2019
K180951Responsive Arthroscopy Suture Anchor SystemJanuary 3, 2019
K180573Responsive Arthroscopy Interference Screw SystemNovember 23, 2018