The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Nexxt Matrixx Stand Alone Cervical-turn Lock (-tl) System.
| Device ID | K200543 |
| 510k Number | K200543 |
| Device Name: | NEXXT MATRIXX Stand Alone Cervical-Turn Lock (-TL) 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 -0566 |
| Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-03-03 |
| Decision Date | 2020-03-23 |