FDA 510(k) Applications Submitted by DAVID J COLLETTE, MD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K121912	07/02/2012	E1 EAR SENSORS	MASIMO CORPORATION
K121914	07/02/2012	MASIMO SET USPO2 PULSE OXIMETRY CABLE	MASIMO CORPORATION
K102769	09/24/2010	NEODENT IMPLANT FOR ORTHODONTIC ANCHORAGE	JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS S
K113596	12/05/2011	MASIMO SET REUSABLE OXIMETRY SENSORS	MASIMO CORPORATION
K110561	02/28/2011	FORTROSS BONE VOID FILLER	PIONEER SURGICAL TECHNOLOGY
K100698	03/11/2010	STCC	CARDINAL SPINE, LLC
K091031	04/10/2009	PIONEER SURGICAL NANOSS BVF-E	PIONEER SURGICAL TECHNOLOGY
K071743	06/27/2007	PILLAR PEDICLE SCREW SYSTEM	THE 4TH COLUMN, LLC
K071796	07/02/2007	CAPSEW PLICATION SYSTEM	CAYENNE MEDICAL, INC.
K082058	07/21/2008	DYNAMATRIX	COOK BIOTECH, INC.
K103084	10/19/2010	NEODENT GRAFT SCREW	JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS S
K073054	10/30/2007	MODIFICATION TO APERFIX FEMORAL IMPLANT WITH INSERTER	CAYENNE MEDICAL, INC.
K083858	12/24/2008	BOND BONE	AUGMA BIOMATERIALS, LTD.
K073685	12/28/2007	OTA COLLAGEN BIOMATERIAL	OSSEOUS TECHNOLOGIES OF AMERICA
K100361	02/12/2010	NANOSS BONE VOID FILLER	PIONEER SURGICAL TECHNOLOGY
K110965	04/06/2011	RENOVIS T 710 LARGE EXTERNAL FIXATION SYSTEM	RENOVIS SURGICAL TECHNOLOGIES, LLC