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