Kinetikos Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinetikos Medical, Inc. - FDA 510(k) Cleared Devices
19
Total
16
Cleared
0
Denied
Kinetikos Medical, Inc. has 16 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Historical record: 16 cleared submissions from 1994 to 2006.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kinetikos Medical, Inc.
19 devices
Cleared
Nov 22, 2006
ECLIPSE TOTAL ANKLE IMPLANT
Orthopedic
154d
Cleared
Oct 05, 2006
KMI CEMENT RESTRICTOR IMPLANT
Orthopedic
132d
Cleared
Sep 06, 2005
MBARESORB IMPLANT
Orthopedic
81d
Cleared
Aug 16, 2004
KMI DISTAL VOLAR RADIUS PLATE SYSTEM
Orthopedic
75d
Cleared
Apr 16, 2004
KATALYST RADIAL HEAD IMPLANT
Orthopedic
220d
Cleared
Mar 01, 2004
KOMPRESSOR SCREW SYSTEM
Orthopedic
17d
Cleared
Feb 06, 2003
KOMPRESSOR SCREW SYSTEM
Orthopedic
45d
Cleared
Feb 05, 2003
UNIVERSAL TOTAL WRIST SYSTEM
Orthopedic
30d
Cleared
Dec 12, 2002
K2 HEMI TOE IMPLANT SYSTEM (FORMERLY ZOBEL GREAT TOE IMPLANT SYSTEM)
Orthopedic
30d
Cleared
May 03, 2002
MODIFICATION TO UNIVERSAL TOTAL WRIST SYSTEM
Orthopedic
72d
Cleared
Aug 17, 1999
KMI WRIST FUSION SYSTEM
Orthopedic
76d
Cleared
Feb 18, 1999
KMI WRIST FUSION SYSTEM
Orthopedic
37d