Medical Device Manufacturer · US , Los Angeles , CA

Kinamed, Inc. - FDA 510(k) Cleared Devices

33 submissions · 29 cleared · Since 1988

Recent clearances: NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM, SUPERCABLE GRIP AND PLATE SYSTEM, NAVIPRO SHOULDER SOFTWARE MODULE

33

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kinamed, Inc. Neurology ✕

5 devices

1-5 of 5

Cleared Apr 05, 2013

NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEM

Neurology · 267d

Cleared May 24, 2005

NAVIPRO SHOULDER SOFTWARE MODULE

Neurology · 46d

Cleared Mar 11, 2004

NAVIPRO KNEE SOFTWARE MODULE

Neurology · 111d

Cleared Jun 03, 2002

Neurology · 88d

Cleared Feb 23, 2001

Neurology · 121d