Interpore Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
25
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K981253ULTRACON ULTRAFILTRATORDecember 11, 1998
K980817PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5September 25, 1998
K972842INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGEOctober 30, 1997
K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEJune 3, 1997
K960945IMZ MEMBRANE TACK SYSTEMMay 24, 1996
K960371INTERPORE THREADED IMPLANTMarch 8, 1996
K955492INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLTJanuary 30, 1996
K952167IMZ BONE TACK SYSTEMNovember 21, 1995
K950165INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO 1000 MICRONS AND 425 TOMarch 28, 1995
K922872INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.July 25, 1994
K922732INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETERFebruary 10, 1994
K913228INTERPORE IMZ CYLINDER IMPLANT SYSTEMOctober 13, 1992
K921246IMZ SURGICAL INSTRUMENT TRAYJune 22, 1992
K912734INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTSJanuary 8, 1992
K904611INTERPORE CYLINDRICAL HEX IMPLANTFebruary 5, 1991
K900793INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEMJuly 27, 1990
K901928INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACHJuly 26, 1990
K883211IMZ O-RING ATTACHMENTNovember 17, 1988
K870331IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTSMarch 2, 1987
K863680IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTSOctober 24, 1986