Medical Device Manufacturer · US , Paramus , NJ

Noviace Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Noviace Corporation has 2 FDA 510(k) cleared medical devices. Based in Paramus, US.

Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Noviace Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Noviace Corporation
2 devices
1-2 of 2
Cleared Apr 01, 2004
OSTEOSORB TACK FIXATION SYSTEM
K030989 · JEY
Orthopedic · 370d
Cleared Oct 06, 2003
NORMED COMPRESSION BONE SCREW SYSTEM
K032634 · JDS
Orthopedic · 41d
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