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 |