Medical Device Manufacturer · CH , Geneva

Spineart - FDA 510(k) Cleared Devices

44 submissions · 44 cleared · Since 2008

Recent clearances: PERLA® TL System, PERLA® TL Posterior Osteosynthesis System, SPINEART Navigation Instrument System

View 44 510(k) Devices ↓

44

Total

44

Cleared

0

Denied

FDA 510(k) Regulatory Record - Spineart General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jan 06, 2016

General & Plastic Surgery · 257d