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Spinefrontier, Inc.

FDA 510(k) & PMA Approved Devices — 15 products

Total Devices15
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K193106 SpineFrontier Lumbar Interbody Fusion Device SystemMAX2020-06-19 View
510(k) K172484 A-CIFT SoloFuseOVE2018-05-08 View
510(k) K132740 SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEMNQW2013-11-26 View
510(k) K123164 SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEMMNH2013-02-15 View
510(k) K121060 SPINE FRONTIER INDUS ACP SYSTEMKWQ2012-07-03 View
510(k) K113518 ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION SYSTEMODP2012-02-16 View
510(k) K111553 SPINEFRONTIER LUMBAR IBF SYSTEMMAX2011-09-28 View
510(k) K102020 VEGA SPAN SPINOUS PROCESS PLATE SYSTEMKWP2010-09-01 View
510(k) K092815 S-LIF INTERVERTEBRAL BODY FUSION DEVICEMAX2010-06-30 View
510(k) K093776 INDUS ANTERIOR CERVICAL PLATE SYSTEMKWQ2010-03-26 View
510(k) K092420 KRD1 PEDICLE SCREW SYSTEMMNI2009-11-19 View
510(k) K091638 DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031MAX2009-09-14 View
510(k) K073232 INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXXKWQ2008-02-20 View
510(k) K071420 CHAMELEON FIXATION SYSTEMMRW2008-01-16 View
510(k) K072289 SPINEFRONTIER DORADO VBRMAX2007-11-01 View
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