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Navbit Pty, Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K243447 Rapid Surgical Plan (RSP-SW-001)LLZ2024-12-05 View
510(k) K200376 Navbit Sprint System- Supine Registration, Navbit Sprint Kit - Lateral RegistrationOLO2020-12-10 View
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