FDA 510(k) Applications Submitted by Ian Helmar
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170676 | 03/06/2017 | HD Lumbar Interbody System | HD LifeSciences LLC |
| K231241 | 04/28/2023 | NanoHive Medical Lumbar Interbody System | NanoHive Medical LLC |
| K223190 | 10/13/2022 | HiveÖ Standalone Cervical System | NanoHive Medical LLC |
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