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Techfit Digital Surgery, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories4
Latest FDA decision2025-10-27
TypeNumberDevice NameCodeDateActions
510(k) K250297 TECHFIT Patient-Specific Cranial SystemGWO2025-10-27 View
510(k) K242263 TECHFIT DISRP® SystemDZJ2024-12-11 View
510(k) K222577 TECHFIT Diagnostic ModelsLLZ2023-01-06 View
510(k) K220199 AFFINITY Proximal Tibia SystemHRS2022-03-21 View
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