Medical Device Manufacturer · US , Moorestown , NJ

The Jerome Group, Inc. - FDA 510(k) Cleared Devices

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

The Jerome Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Moorestown, US.

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

Browse the FDA 510(k) cleared devices submitted by The Jerome Group, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The Jerome Group, Inc.
2 devices
1-2 of 2
Cleared Apr 12, 2004
CERAMIC TIPPED SKULL PIN
K040363 · LYT
Orthopedic · 59d
Cleared Feb 21, 2003
JEROME GLASS RING
K023959 · HAX
Neurology · 86d
Filters
Filter by Specialty
All2 Neurology 1 Orthopedic 1