The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Trelloss™-l Mpf.
| Device ID | K192687 |
| 510k Number | K192687 |
| Device Name: | TrellOss™-L MPF |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-09-26 |
| Decision Date | 2020-01-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TRELLOSS 88401530 not registered Live/Pending |
Zimmer Biomet Spine, Inc. 2019-04-25 |