FDA 510(k) Applications Submitted by ROBERT J SLOMOFF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K032448	08/08/2003	ALTATEC CERAMIC ABUTMENT	ALTATEC BIOTECHNOLOGIES
K974358	11/19/1997	FRIALIT -2 SCREW	FRIATEC AG
K022425	07/24/2002	SCREWLINE	ALTATEC BIOTECHNOLOGIES N.A., INC.
K963520	09/03/1996	IMZ TWIN PLUS SCREW	IMZ, GMBH
K963521	09/03/1996	IMZ TWIN PLUS - CYLINDER	IMZ, GMBH
K963522	09/03/1996	IMZ 2000 INTERLOCK 12/3 - SCREW	IMZ, GMBH
K973924	10/15/1997	FRIOS BONESHIELD	FRIATEC AG
K974359	11/19/1997	FRIALIT-2 CYLINDER	FRIATEC AG
K945847	11/30/1994	FRIALIT(R)-2 STEPPED SCREW WITH DEEP PROFILE SURFACE	FRIATEC MEDICAL INC., USA
K945848	11/30/1994	FRIALIT(R)-2 DENTAL IMPLANT	FRIATEC MEDICAL INC., USA
K945849	11/30/1994	FRIALIT(R)-2 STEPPED CYLINDER WITH FRIOS(R) TI-COATING	FRIATEC MEDICAL INC., USA
K974628	12/11/1997	FRIALIT-2 PROTECT ABUTMENT	FRIATEC AG