COMPANY
OrthoNovis
Timeline
- FDA FDA 510(k) clearance: Cannulated Screw and Kirschner (K wire) System — K252758, Oct 2, 2025. Applicant at approval: Orthonovis, Inc. source ↗
- FDA FDA 510(k) clearance: BPS Wrist Fracture System — K250498, Mar 17, 2025. Applicant at approval: Orthonovis, Inc. source ↗
- FDA FDA 510(k) clearance: BPS - Bone Fragment Fixation Plates, Screws and Washers — K250055, Feb 6, 2025. Applicant at approval: Orthonovis, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: Cannulated Screw and Kirschner (K wire) System — K252758, Oct 2, 2025. Applicant at approval: Orthonovis, Inc. source ↗
- FDA 510(k) clearance: BPS Wrist Fracture System — K250498, Mar 17, 2025. Applicant at approval: Orthonovis, Inc. source ↗
- FDA 510(k) clearance: BPS - Bone Fragment Fixation Plates, Screws and Washers — K250055, Feb 6, 2025. Applicant at approval: Orthonovis, Inc. source ↗
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