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SpineFrontier, Inc.: 510(k) Clearances

24 510(k) clearances from Nov 1, 2007 to Jun 19, 2020, newest first. Showing 1 to 24.

What this list covers: FDA records filed under the name "SpineFrontier, Inc." and its spelling variant "Spinefrontier".

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K-NumberDeviceDate
K193106SpineFrontier Lumbar Interbody Fusion Device SystemJun 19, 2020
K172484A-CIFT SoloFuseMay 8, 2018
K151198A-CIFT SoloFuseJul 17, 2015
K142504SpineFrontier Lumbar Interbody Fusion Device SystemMay 13, 2015
K150017SpineFrontier SIJFuse Sacroiliac Joint Fusion Device SystemApr 24, 2015
K143377PedFuse Pedicle Screw SystemFeb 12, 2015
K141333ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICENov 25, 2014
K142026SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICEOct 20, 2014
K141337ARENA-CSep 8, 2014
K133153SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEMMay 14, 2014
K131880SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEMJan 3, 2014
K132740SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEMNov 26, 2013
K123164SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEMFeb 15, 2013
K121060SPINE FRONTIER INDUS ACP SYSTEMJul 3, 2012
K113518ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION SYSTEMFeb 16, 2012
K111553SPINEFRONTIER LUMBAR IBF SYSTEMSep 28, 2011
K102020VEGA SPAN SPINOUS PROCESS PLATE SYSTEMSep 1, 2010
K092815S-LIF INTERVERTEBRAL BODY FUSION DEVICEJun 30, 2010
K093776INDUS ANTERIOR CERVICAL PLATE SYSTEMMar 26, 2010
K092420KRD1 PEDICLE SCREW SYSTEMNov 19, 2009
K091638DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031Sep 14, 2009
K073232INDUS ANTERIOR CERVICAL PLATE SYSTEM, MODEL IM3XXXFeb 20, 2008
K071420CHAMELEON FIXATION SYSTEMJan 16, 2008
K072289SPINEFRONTIER DORADO VBRNov 1, 2007

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.