Otto Bock Orthopedic Industry, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Otto Bock Orthopedic Industry, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Otto Bock Orthopedic Industry, Inc. has 6 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 6 cleared submissions from 1995 to 2000. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Otto Bock Orthopedic Industry, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Otto Bock Orthopedic Industry, Inc.
6 devices
Cleared
Oct 24, 2000
EVANTGARDE/ENDEAVOR POWERED WHEELCHAIR
Physical Medicine
231d
Cleared
Sep 18, 2000
RAEBBITT/EVOLUTION POWERED WHEELCHAIR
Physical Medicine
202d
Cleared
Mar 08, 2000
VOYAGER/VIPER WHEELCHAIR
Physical Medicine
22d
Cleared
Mar 03, 2000
PROTEGE WHEELCHAIR
Physical Medicine
9d
Cleared
Jul 08, 1999
C-LEG (3C100)
Physical Medicine
62d
Cleared
May 12, 1995
AVANTGARDE
Physical Medicine
22d