FDA 510(k) Applications Submitted by DAVID P BALDING

FDA 510(k) Number Submission Date Device Name Applicant
K040315 02/09/2004 MYOHEALTH CLENCHING INHIBITOR MCI-MYOHEALTH SYSTEMS
K952167 05/08/1995 IMZ BONE TACK SYSTEM INTERPORE INTL.
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.


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