FDA 510(k) Applications Submitted by Chloe Lance
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220096 | 01/12/2022 | Genesys Spine 3DP Lumbar Interbody System | Genesys Spine |
| K192678 | 09/26/2019 | Genesys Spine Binary« Lumbar Plate System | Genesys Spine |
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