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Responsive Arthroscopy, Inc.

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Thunderbolt System (K261632)Responsive Arthroscopy, Inc.2026-07-20
Osprey Suture Anchor (K243726)Responsive Arthroscopy, Inc.2025-01-30

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Every clearance here is in the API, with alerts when new ones post.