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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.
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