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FDA 510(k) Applications Submitted by SIMON FITZER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050170
01/26/2005
FORTOSS VITAL BONE GRAFT SUBSTITUTE
BIOCOMPOSITES LTD.
K071091
04/18/2007
MODIFICATION TO BILOK SCREW
BIOCOMPOSITES LTD.
K071115
04/20/2007
MODIFICATION TO BILOK ST SCREW
BIOCOMPOSITES LTD.
K061311
05/10/2006
ALLOGRAN-R
BIOCOMPOSITES LTD.
K991662
05/14/1999
TITANIUM HARTSHILL SYSTEM
SURGICRAFT LTD.
K081428
05/21/2008
MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR
BIOCOMPOSITES LTD.
K061949
07/10/2006
DOUBLEPLAY SUTURE ANCHOR
BIOCOMPOSITES LTD.
K071952
07/16/2007
GRAFTLOCK SCREW, ST SCREW
BIOCOMPOSITES LTD.
K072127
08/02/2007
DOMINATOR
BIOCOMPOSITES LTD.
K982719
08/04/1998
THE BONE TIE
SURGICRAFT LTD.
K082381
08/19/2008
GENEX
BIOCOMPOSITES LTD.
K212721
08/27/2021
Genex Bone Graft Substitute
Biocomposites Ltd
K073341
11/28/2007
GENEX PUTTY
BIOCOMPOSITES LTD.
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