Medical Device Manufacturer · US , Ormond Beach , FL

Citieffe - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Citieffe Orthopedic ✕
3 devices
1-3 of 3
Cleared Jun 05, 2012
CITIEFFE-TITANIUM CANNULATED SCREW
K113388 · HWC
Orthopedic · 202d
Cleared May 01, 2012
EXTERNAL FIXATOR ST.A R 90 F4
K113384 · KTT
Orthopedic · 167d
Cleared Mar 15, 2012
CITIEFFE TITANIUM NAILING SYSTEM
K113387 · HSB
Orthopedic · 120d
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