The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Nexxt Matrixx Stand Alone Cervical System.
Device ID | K190546 |
510k Number | K190546 |
Device Name: | NEXXT MATRIXX Stand Alone Cervical System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
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 | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-03-05 |
Decision Date | 2019-05-31 |