The following data is part of a premarket notification filed by Nexxt Spine Llc with the FDA for Honour Spacer System.
Device ID | K120345 |
510k Number | K120345 |
Device Name: | HONOUR SPACER SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | NEXXT SPINE LLC PO BOX 566 Chesterland, OH 44026 |
Contact | Karen E Warden |
Correspondent | Karen E Warden NEXXT SPINE LLC PO BOX 566 Chesterland, OH 44026 |
Product Code | ODP |
Subsequent Product Code | MAX |
Subsequent Product Code | MQP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-03 |
Decision Date | 2012-06-13 |
Summary: | summary |