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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