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 |