The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Saxxony™ Posterior Cervical Thoracic System.
Device ID | K182508 |
510k Number | K182508 |
Device Name: | Saxxony™ Posterior Cervical Thoracic System |
Classification | Posterior Cervical Screw System |
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 | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-12 |
Decision Date | 2018-11-13 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SAXXONY 87560976 5723022 Live/Registered |
Nexxt Spine, LLC 2017-08-08 |
SAXXONY 86169609 not registered Dead/Abandoned |
Nexxt Spine, LLC 2014-01-19 |