FDA 510(k) Applications Submitted by JASON GROMEK

FDA 510(k) Number Submission Date Device Name Applicant
K150788 03/25/2015 Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral Body Fusion Devices, Talos -C(HA) Cervical Intervertebral Body Fusion Devices MEDITECH SPINE, LLC
K142345 08/22/2014 Talos-C(HA) Cervical Intervertebral Body Fusion Devices MEDITECH SPINE, LLC


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