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FDA 510(k) Applications Submitted by ALPHATEC/NEXMED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K042201
08/13/2004
NOVEL VBR SPINAL SYSTEM
ALPHATEC/NEXMED
K042440
09/09/2004
ALPHATEC FEMORAL TROCHANTERIC NAIL (FTN) SYSTEM
ALPHATEC/NEXMED
K050390
02/16/2005
TAMARACK ANTERIOR THORACOLUNBAR
ALPHATEC/NEXMED
K050078
01/13/2005
ROC LUMBAR PLATING SYSTEM
ALPHATEC/NEXMED
K050553
03/03/2005
NOVEL VBR SPINAL SYSTEM
ALPHATEC/NEXMED
K050830
04/01/2005
ZODIAC SPINAL FIXATION SYSTEM
ALPHATEC/NEXMED
K051286
05/18/2005
ZODIAC SPINAL FIXATION SYSTEM
ALPHATEC/NEXMED
K042252
08/20/2004
NEXFLEX TOTAL HIP SYSTEM
ALPHATEC/NEXMED
K042673
09/29/2004
ZODIAC POLYAXIAL SPINAL FIXATION SYSTEM
ALPHATEC/NEXMED
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