Medical Device Manufacturer · US , Irvine , CA

Interpore Cross Intl. - FDA 510(k) Cleared Devices

39 submissions · 38 cleared · Since 1998

39

Total

38

Cleared

0

Denied

FDA 510(k) Regulatory Record - Interpore Cross Intl. Orthopedic ✕

34 devices

1-12 of 34

Cleared May 27, 2005

Orthopedic · 52d

Cleared Feb 18, 2005

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