The following data is part of a premarket notification filed by Zavation Medical Products, Llc with the FDA for Ti 3z Interbody System.
| Device ID | K180076 |
| 510k Number | K180076 |
| Device Name: | Ti 3Z Interbody System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Zavation Medical Products, LLc 220 Lakeland Parkway Flowood, MS 39232 |
| Contact | Katie Motley |
| Correspondent | Katie Motley Zavation Medical Products, LLc 220 Lakeland Parkway Flowood, MS 39232 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-01-10 |
| Decision Date | 2018-07-27 |
| Summary: | summary |