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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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