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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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