The following data is part of a premarket notification filed by Genesys Spine with the FDA for Genesys Spine 3dp Lumbar Interbody System.
| Device ID | K182987 |
| 510k Number | K182987 |
| Device Name: | Genesys Spine 3DP Lumbar Interbody System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Genesys Spine 1250 South Capital Of Texas Highway, Building 3 Suite 600 Austin, TX 78746 |
| Contact | William W. Sowers |
| Correspondent | William W. Sowers Genesys Spine 1250 South Capital Of Texas Highway, Building 3 Suite 600 Austin, TX 78746 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-10-29 |
| Decision Date | 2019-12-12 |