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Responsive Arthroscopy, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2026-07-20
TypeNumberDevice NameCodeDateActions
510(k) K261632 Thunderbolt SystemMBI2026-07-20 View
510(k) K243726 Osprey Suture AnchorMBI2025-01-30 View
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