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FDA 510(k) Applications Submitted by ROBERT 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
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