Medical Device Manufacturer · CH , Brugg

Naviswiss AG - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2020
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Naviswiss AG Radiology ✕
1 devices
1-1 of 1
Cleared Oct 05, 2021
NAVIPLAN - CT Planning Software for Total Hip Replacement
K211429 · LLZ
Radiology · 151d
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