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 |