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FDA 510(k) Applications Submitted by SANACOR
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090477
02/24/2009
ALPINE PEDICLE SCREW SYSTEM
SANACOR
K070933
04/03/2007
LOWTOP PEDICLE SCREW SYSTEM
SANACOR
K073500
12/13/2007
ACTIVE ANTERIOR CERVICAL PLATE SYSTEM
SANACOR
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