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FDA 510(k) Applications Submitted by REBECCA BLANK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120807
03/16/2012
SYNTHES MULTILOC HUMERAL NAILING SYSTEM
SYNTHES USA PRODUCTS LLC
K111230
05/02/2011
SYNTHES 3.5MM LOW PROFILE CORTICAL SCREW
SYNTHES (USA) PRODUCTS LLC
K112583
09/06/2011
SYNTHES CORTICAL SCREWS
SYNTHES (USA) PRODUCTS LLC
K113364
11/15/2011
2.7MM LCP ULNA OSTEOTOMY SYSTEM
SYNTHES (USA) PRODUCTS LLC
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