The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Nexxt Matrixx System.
Device ID | K200969 |
510k Number | K200969 |
Device Name: | NEXXT MATRIXX System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Nexxt Spine LLC 14425 Bergen Blvd, Suite B Noblesville, IN 46060 |
Contact | Andy Elsbury |
Correspondent | Karen E. Warden BackRoads Consulting PO BOX 566 Chesterland, OH 44026 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-04-13 |
Decision Date | 2020-05-21 |