FDA 510(k) Applications Submitted by HOWARD 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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