FDA 510(k) Applications Submitted by CHERYL L WAGONER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100210	01/25/2010	TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T	TRANS1 INCORPORATED
K141078	04/25/2014	ORTHOFIX TL-HEX TRUE LOK HEXALOBE SYSTEM (TL-HEX)	ORTHOFIX SRL
K141760	07/01/2014	ORTHOFIX GALAXY WRIST	ORTHOFIX SRL
K092124	07/15/2009	AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II	TRANS1 INCORPORATED
K142052	07/28/2014	ORTHOFIX GALAXY UNYCO DIAPHYSEAL TIBIA KIT	ORTHOFIX SRL
K102334	08/17/2010	TRANS1 AXIALIF PLUS	TRANS1 INCORPORATED
K120991	04/02/2012	TRANS1 INTERBODY FUSION SYSTEM	TRANS1 INCORPORATED
K123997	12/26/2012	TRANS1LATERAL INTERBODY FUSION SYSTEM	TRANS1, INC.