The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Nexxt Matrixx Stand Alone Alif System.
| Device ID | K202230 |
| 510k Number | K202230 |
| Device Name: | NEXXT MATRIXX Stand Alone ALIF System |
| Classification | Intervertebral Fusion Device With Integrated Fixation, 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 | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-08-07 |
| Decision Date | 2020-12-15 |
| Summary: | summary |