Interpore Cross Intl. - FDA 510(k) Cleared Devices
39
Total
38
Cleared
0
Denied
Interpore Cross Intl. has 38 FDA 510(k) cleared orthopedic devices. Based in Irvine, US.
Historical record: 38 cleared submissions from 1998 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.
39 devices
Cleared
May 27, 2005
PEEK CAS
Orthopedic
52d
Cleared
Feb 18, 2005
INTERGRO DBM
Orthopedic
655d
Cleared
Dec 29, 2004
TITANIUM MESH IMPLANT
Orthopedic
216d
Cleared
Dec 21, 2004
MODIFICATION TO ALTIUS OCT SYSTEM
Orthopedic
29d
Cleared
Nov 04, 2004
C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
27d
Cleared
Aug 27, 2004
EXPANDABLE PEEK VBR IMPLANT
Orthopedic
140d
Cleared
Jul 19, 2004
C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
17d
Cleared
Jul 01, 2004
SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION...
Orthopedic
30d
Cleared
Apr 14, 2004
ALTIUS OCT SYSTEM
Orthopedic
114d
Cleared
Apr 08, 2004
MODIFICATION TO GEO STRUCTURE
Orthopedic
73d
Cleared
Sep 05, 2003
TI FENESTRATED PLATE
Orthopedic
88d
Cleared
Aug 08, 2003
INTERPORE CROSS CEMENT RESTRICTOR
Orthopedic
31d
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