FDA 510(k) Applications Submitted by ERIN MALLOY

FDA 510(k) Number Submission Date Device Name Applicant
K060247 01/31/2006 LIFE SPINE CEMENT RESTRICTOR LIFE SPINE
K061364 05/16/2006 PILOT POSTERIOR LUMBAR PLATING SYSTEM LIFE SPINE
K061600 06/08/2006 ARX SPINAL SYSTEM LIFE SPINE
K061698 06/16/2006 MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR LIFE SPINE
K062643 09/06/2006 KINETIC ANTERIOR CERVICAL PLATE LIFE SPINE
K062831 09/20/2006 MODIFICATION TO LIFE SPINE NEO ANTERIOR CERVICAL PLATE SYSTEM LIFE SPINE


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