FDA 510(k) Applications Submitted by ALBERT ENAYATI

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010118	01/16/2001	NORMED MANDIBULAR FIXATION SYSTEM	OSTEOMEDICS, INC.
K030989	03/28/2003	OSTEOSORB TACK FIXATION SYSTEM	NOVIACE CORPORATION
K011118	04/12/2001	NORMED EXTREMITY TITANIUM HAND AND SMALL FRAGMENT SYSTEM	OSTEOMEDICS
K021341	04/29/2002	NORMED BONE TRANSPORT DISTRACTION DEVICE	OSTEOMEDICS, INC.
K021342	04/29/2002	NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR	OSTEOMEDICS, INC.
K022230	07/10/2002	NORMED MINI EXTERNAL FIXATOR SYSTEM	OSTEOMEDICS, INC.
K022231	07/10/2002	NORMED DISTAL RADIUS RECONSTRUCTION SYSTEM	OSTEOMEDICS, INC.
K022323	07/17/2002	NORMED TITANIUM RONDO FIX FUSION PLATES AND SCREW SYSTEM	OSTEOMEDICS, INC.
K022324	07/17/2002	NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM	OSTEOMEDICS, INC.
K022325	07/17/2002	NORMED TITANIUM OSTEOTOMY PLATING SYSTEM	OSTEOMEDICS, INC.
K032634	08/26/2003	NORMED COMPRESSION BONE SCREW SYSTEM	NOVIACE CORPORATION