Medical Device Manufacturer · US , Cambridge , MA

Genesis Orthopedics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 0 cleared · Since 1995
2
Total
0
Cleared
0
Denied

Genesis Orthopedics, Inc. has 0 FDA 510(k) cleared medical devices. Based in Cambridge, US.

Historical record: 0 cleared submissions from 1995 to 1995. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Genesis Orthopedics, Inc.
2 devices
1-2 of 2
Cleared Dec 19, 1995
GO INTRAMEDULLARY NAIL LOCKING SCREW
K954511 · HWC
Orthopedic · 82d
Cleared Dec 08, 1995
GO UNIVERSALK-WIRE FLUTED DRILL
K954543 · HTY
Orthopedic · 71d
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