Scholten Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NOVATOME, MODEL: SU101-50, SCHOLTEN FRAME, SYS, ANGIOGRAPHIC, SINGLE-OR BI-PLANE RADIOGRAPHIC
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Scholten Surgical Instruments, Inc. General & Plastic Surgery ✕
4 devices