Navbit Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Navbit Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Rapid Surgical Plan (RSP-SW-001), Navbit Sprint System- Supine Registration, Navbit Sprint Kit - Lateral Registration
2
Total
2
Cleared
0
Denied
Navbit Pty, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Crows Nest, AU.
Latest FDA clearance: Dec 2024. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Navbit Pty, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Secure BioMed Evaluations and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Navbit Pty, Ltd.
2 devices