FDA 510(k) Applications Submitted by John Sullivan

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180364	02/12/2018	HD LifeSciences Cervical IBFD System	HD LifeSciences LLC
K200541	03/03/2020	HiveÖ Stand-alone Anterior Lumbar Interbody System	HD LifeSciences LLC
K091638	06/04/2009	DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031	SPINEFRONTIER, INC.
K102020	07/19/2010	VEGA SPAN SPINOUS PROCESS PLATE SYSTEM	SPINEFRONTIER, INC.
K092420	08/06/2009	KRD1 PEDICLE SCREW SYSTEM	SPINEFRONTIER, INC.
K092815	09/14/2009	S-LIF INTERVERTEBRAL BODY FUSION DEVICE	SPINEFRONTIER, INC.
K213266	09/30/2021	Inspan ScrewLES Fusion System	LESpine Innovations, LLC
K093776	12/08/2009	INDUS ANTERIOR CERVICAL PLATE SYSTEM	SPINEFRONTIER, INC.