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FDA 510(k) Applications Submitted by REBECCA BROOK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120370
02/06/2012
VIVACIT-E VITAMIN E HIGHLY CROSSLINKED POLYETHYLENE LINERS
ZIMMER, INC.
K101229
05/03/2010
LONGEVITY IT HIGHLY CROSSLINKED POLYETHYLENE ELEVATED LINERS, CONTINUUM ACETABULAR SYSTEM AND TRILOGY INTEGRATED TAPER
ZIMMER, INC.
K123019
09/28/2012
LONGEVITY IT HIGHLY CROSSLINKED POLYETHYENE LINERS
ZIMMER, INC.
K103662
12/15/2010
CONTINUUM AND TRILOGY INTEGRATED TAPER (IT) ACETABULAR SYSTEMS; LONGEVITY IT HIGHLY CROSSLINKED POLYETHYLENE ELEVATED LI
ZIMMER, INC.
K070285
01/29/2007
LIFE SPINE ANTERIOR CERVICAL PLATE SYSTEM
LIFE SPINE
K080411
02/15/2008
PLATEAU SPACER SYSTEM
LIFE SPINE
K080502
02/25/2008
MODIFICATION TO:PILOT SPINAL SYSTEM
LIFE SPINE
K080767
03/18/2008
CONQUEST SPINAL SYSTEM
LIFE SPINE
K130899
04/01/2013
BIOLOX DELTA CERAMIC FEMORAL HEADS
ZIMMER GMBH
K070995
04/09/2007
ARX-LINK CROSS CONNECTOR
LIFE SPINE
K073274
11/21/2007
SPINAL SPHERE SYSTEM
LIFE SPINE
K063601
12/04/2006
PILOT SPINAL SYSTEM
LIFE SPINE
K073479
12/11/2007
KINETIC-SL ANTERIOR CERVICAL PLATE SYSTEM
LIFE SPINE
K073480
12/11/2007
LIFE SPINE CROSS CONNECTOR
LIFE SPINE
K083865
12/29/2008
PILOT SPINAL SYSTEM
LIFE SPINE
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