Medical Device Manufacturer · US , Jacksonville , FL

Arftx Medical, LLC

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Arftx Medical, LLC — FDA 510(k) Submissions

Arftx Medical, LLC has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spinal Vertebral Body Replacement Device . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Orthopedic 1