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Pinnacle Spine Group, LLC

12 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
InFill® Interbody Fusion Device (K172349)Pinnacle Spine Group, LLC2017-12-14
InFill Interbody Fusion Device (K152259)Pinnacle Spine Group, LLC2015-11-19
InFill Interbody Fusion Devices (K151184)Pinnacle Spine Group, LLC2015-07-14
InFill Interbody Fusion Devices (K150206)Pinnacle Spine Group, LLC2015-04-03
InFill Graft Delivery System (K143488)Pinnacle Spine Group, LLC2014-12-17
INFILL CERVICAL (K140066)Pinnacle Spine Group, LLC2014-05-05
INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL 44-TLIF CONTOUR OBLIQUE AND THE INFILL 60 (K133721)Pinnacle Spine Group, LLC2014-03-31
INFILL OBLIQUE TLIF DEVICE (K124012)Pinnacle Spine Group, LLC2013-06-04
INFILL GRAFT DELIVERY SYSTEM (K121476)Pinnacle Spine Group, LLC2012-08-29
INFILL INTERVERTEBRAL BODY FUSION DEVICE (K121733)Pinnacle Spine Group, LLC2012-07-13
INFILL GRAFT DELIVERY SYSTEM (K111632)Pinnacle Spine Group, LLC2011-08-11
INFILL INTERVERTEBRAL BODY FUSION DEVICE (K103729)Pinnacle Spine Group, LLC2011-04-18

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Every clearance here is in the API, with alerts when new ones post.