Depuy, Inc. - FDA 510(k) Cleared Devices
303
Total
239
Cleared
0
Denied
Depuy, Inc. has 239 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 239 cleared submissions from 1976 to 2005.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
303 devices
Cleared
Mar 14, 2005
PINNACLE CONSTRAINED ACETABULAR LINERS
Orthopedic
129d
Cleared
Dec 08, 2004
LPS UPPER EXTREMITY
Orthopedic
71d
Cleared
Jul 22, 2004
LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY
Orthopedic
87d
Cleared
Jul 01, 2004
LPS
Orthopedic
192d
Cleared
May 28, 2004
DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044...
Orthopedic
87d
Cleared
Nov 18, 2003
DELTA SHOULDER
Orthopedic
559d
Cleared
Nov 14, 2003
DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS
Orthopedic
29d
Cleared
Sep 26, 2003
DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS
Orthopedic
74d
Cleared
May 20, 2002
AGILITY ANKLE REVISION PROSTHESIS
Orthopedic
90d
Cleared
Sep 07, 2001
ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING
Orthopedic
88d
Cleared
Jun 27, 2001
ORTHOGENESIS LPS SYSTEM
Orthopedic
259d
Cleared
Aug 29, 2000
DEPUY NEUFLEX PIP FINGER
Orthopedic
67d
Looking for a specific device from Depuy, Inc.? Search by device name or K-number.
Search all Depuy, Inc. devices