FDA 510(k) Applications Submitted by HD LifeSciences LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170676 | 03/06/2017 | HD Lumbar Interbody System | HD LifeSciences LLC |
| K180364 | 02/12/2018 | HD LifeSciences Cervical IBFD System | HD LifeSciences LLC |
| K200541 | 03/03/2020 | HiveÖ Stand-alone Anterior Lumbar Interbody System | HD LifeSciences LLC |
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