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 |