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FDA 510(k) Applications Submitted by HT Medical, LLC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170318
02/01/2017
NeoFuse Ti3D PLIF/TLIF/Cervical Interbody
HT Medical, LLC
K170511
02/21/2017
NeoFuse HA Enhanced PLIF/TLIF
HT Medical, LLC
K153615
12/17/2015
NeoFuse HA Enhanced PLIF/TLIF
HT MEDICAL, LLC
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