Depuyacromed - FDA 510(k) Cleared Devices
48
Total
48
Cleared
0
Denied
Depuyacromed has 48 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.
Historical record: 48 cleared submissions from 1999 to 2004.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
48 devices
Cleared
Apr 02, 2004
EAGLE ANTERIOR CERVIAL PLATE SYSTEM
Orthopedic
64d
Cleared
Jun 23, 2003
DEPUY ACROMED VBR SYSTEM
Orthopedic
27d
Cleared
Apr 10, 2003
DEPUY ACROMED VBR SYSTEM
Orthopedic
24d
Cleared
Feb 26, 2003
MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWS
Orthopedic
21d
Cleared
Feb 14, 2003
SURGICAL TITANIUM MESH SYSTEM
Orthopedic
21d
Cleared
Feb 05, 2003
SUMMIT OCT SPINAL SYSTEM MINIPOLYAXIAL SCREWS
Orthopedic
23d
Cleared
Jan 29, 2003
DEVEX MESH SYSTEM
Orthopedic
72d
Cleared
Jan 28, 2003
MONARCH SPINE SYSTEM
Orthopedic
29d
Cleared
Jan 23, 2003
MOSS MIAMI SPINAL SYSTEM PIN NUT
Orthopedic
70d
Cleared
Dec 11, 2002
BOWTI ANTERIOR BUTTRESS STAPLE SYSTEM
Orthopedic
254d
Cleared
Nov 13, 2002
MODIFICATION TO MONARCH SPINE SYSTEM
Orthopedic
29d
Cleared
Aug 27, 2002
5.0 MM DIAMETER POLYAXIAL SCREWS (MOSS MIAMI 6.35MM SYSTEM)
Orthopedic
20d
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