The following data is part of a premarket notification filed by Omnia Medical, Llc with the FDA for Omnia Medical Tibrid Cervical Cage, Omnia Medical Tibrid Lateral Cage, Omnia Medical Tibrid Alif Cage, Omnia Medical Tibrid Plif Cage, Omnia Medical Tibrid Tlif Cage.
Device ID | K190363 |
510k Number | K190363 |
Device Name: | Omnia Medical TiBrid Cervical Cage, Omnia Medical TiBrid Lateral Cage, Omnia Medical TiBrid ALIF Cage, Omnia Medical TiBrid PLIF Cage, Omnia Medical TiBrid TLIF Cage |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Omnia Medical, LLC 6 Canyon Rd Suite 300 Morgantown, WV 26508 |
Contact | Troy Schifano |
Correspondent | Daniel Johnson JALEX Medical 30311 Clemens Rd Suite 5D Westlake, OH 44145 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-02-15 |
Decision Date | 2020-02-21 |