Interpore Cross Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
39
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K050861PEEK CASMay 27, 2005
K031399INTERGRO DBMFebruary 18, 2005
K041407TITANIUM MESH IMPLANTDecember 29, 2004
K043229MODIFICATION TO ALTIUS OCT SYSTEMDecember 21, 2004
K042798C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEMNovember 4, 2004
K040928EXPANDABLE PEEK VBR IMPLANTAugust 27, 2004
K041794C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEMJuly 19, 2004
K041449SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEATJuly 1, 2004
K033961ALTIUS OCT SYSTEMApril 14, 2004
K040168MODIFICATION TO GEO STRUCTUREApril 8, 2004
K031772TI FENESTRATED PLATESeptember 5, 2003
K032095INTERPORE CROSS CEMENT RESTRICTORAugust 8, 2003
K023908INTERPORE CROSS CEMENT RESTRICTORMay 16, 2003
K022143INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)January 23, 2003
K022048INTERPORE CROSS INTERNATIONAL (ICI) OCCIPITO-CERVICO-THORACIC (OCT) ROD AND PLATE SYSTEMDecember 4, 2002
K022348ACCESS CONCENTRATION SYSTEM, MODEL ACC-100, ACCESS DISPOSABLE SET, MODEL ADS-2000August 15, 2002
K012406ACCESS SEQUESTRATION SYSTEMMarch 26, 2002
K020204TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODELS 8123, 8124, 8132, 8133, 8156, 8February 21, 2002
K020048MODIFICATION TO GEO STRUCTUREFebruary 6, 2002
K014145MODIFICATION TO TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODEL 8130, 8131January 17, 2002