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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