FDA 510(k) Applications Submitted by HOWARD A MERCER

FDA 510(k) Number Submission Date Device Name Applicant
K040364 02/13/2004 MEDPOR CRANIOFACIAL IMPLANTS WITH EMBEDDED TITANIUM MESH POREX SURGICAL, INC.
K010902 03/26/2001 MEDPOR QUAD MOTILITY IMPLANT POREX SURGICAL, INC.
K040851 03/31/2004 MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM POREX SURGICAL, INC.
K021357 04/29/2002 MEDPOR PLUS ORBITAL VOLUME REPLACEMENT IMPANT POREX SURGICAL, INC.
K971583 04/30/1997 MEDPOR OCULAR SCREW AND ACCEOSSORIES POREX TECHNOLOGIES CORP.
K972034 06/02/1997 MEDPOR OCULAR CONFORMER POREX SURGICAL, INC.
K982040 06/10/1998 MEDPOR SURGICAL GRANULE IMPLANTS POREX SURGICAL, INC.
K012108 07/06/2001 MEDPOR COATED TEAR DRAIN POREX SURGICAL, INC.
K012350 07/25/2001 MEDPOR PLUS SURGICAL IMPLANT BIOMATERIAL POREX SURGICAL, INC.
K002586 08/21/2000 MEDPOR PTERIONAL SURGICAL IMPLANT POREX SURGICAL PRODUCTS GROUP
K960859 03/01/1996 MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES POREX TECHNOLOGIES CORP. OF GEORGIA
K981374 04/16/1998 POREX NOSTRIL RETAINERS POREX SURGICAL, INC.
K954939 10/30/1995 MEDPOR OCULAR SCREW & ACCESSORIES POREX SURGICAL, INC.


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