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FDA 510(k) Applications Submitted by INTERPORE INTL.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960371
01/26/1996
INTERPORE THREADED IMPLANT
INTERPORE INTL.
K980817
03/03/1998
PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L
INTERPORE INTL.
K972842
08/01/1997
INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
INTERPORE INTL.
K955492
12/01/1995
INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT
INTERPORE INTL.
K960945
03/08/1996
IMZ MEMBRANE TACK SYSTEM
INTERPORE INTL.
K981253
04/06/1998
ULTRACON ULTRAFILTRATOR
INTERPORE INTL.
K971036
03/20/1997
ODONTIT AUTOGENOUS BONE COLLECTION DEVICE
INTERPORE INTL.
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