FDA 510(k) Applications Submitted by Benjamin V. Keller
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180056 | 01/08/2018 | Genesys Spine AIS-C Cervical Anchored Interbody System | Genesys Spine |
| K181295 | 05/16/2018 | Genesys Spine AIS-C Cervical Stand-Alone System | Genesys Spine |
| K191489 | 06/04/2019 | Genesys Spine 3DP Cervical Interbody System | Genesys Spine |
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