Atlas FDA

Interpore Intl.

12 FDA 510(k) clearances · PMA applicant

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RecordFirmDate
PRO OSTEON 500 BONE GRAFT SUBSTITUTE (P860005/S012)Interpore Intl.2002-05-31
PRO OSTEON 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUE BLOCKS & GRANULES (P860005/S011)Interpore Intl.1999-05-25
PRO OSTEON IMPLANT 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUTE BLOCKS & GRANULES (P860005/S009)Interpore Intl.1998-04-28
PRO OSTEON IMPLANT 500 POROUS CORALLINE HYDROXYAPATITE BONE GRAFT SUBSTITUTE (P860005/S010)Interpore Intl.1998-01-08
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500) (P860005/S008)Interpore Intl.1997-09-11
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500) (P860005/S007)Interpore Intl.1997-05-30
PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500) (P860005/S005)Interpore Intl.1996-07-18
INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX (P860005/S004)Interpore Intl.1994-08-08
INTERPORE PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FILLER (P860005/S001)Interpore Intl.1994-03-17
INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX (P860005/S003)Interpore Intl.1994-03-17
INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX (P860005/S002)Interpore Intl.1993-11-17
PRO OSTEON IMPLANT 500 HYDROXYAPATITE BONE VOID FILLER (P860005)Interpore Intl.1992-10-29

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Every clearance here is in the API, with alerts when new ones post.