The following data is part of a premarket notification filed by U&i Corporation with the FDA for Velofix Tlif Cage.
| Device ID | K183243 |
| 510k Number | K183243 |
| Device Name: | Velofix TLIF Cage |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | U&i Corporation 20, Sandan-ro 76beon-gil(Rd) Uijeongbu-si, KR 11781 |
| Contact | Jee Ae Bang |
| Correspondent | Jee-ae Bang U&i Corporation 20, Sandan-ro 76beon-gil(Rd) Uijeongbu-si, KR 11781 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-11-21 |
| Decision Date | 2019-07-10 |