The following data is part of a premarket notification filed by Additive Implants, Llc with the FDA for Cervical Spacer.
| Device ID | K182477 |
| 510k Number | K182477 |
| Device Name: | Cervical Spacer |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | Additive Implants, LLC 3101 E. Shea Blvd, Suite 114 Pheonix, AZ 85028 |
| Contact | Jeff Horn |
| Correspondent | Karen E. Warden BackRoads Consulting 12520 Heath Road Chesterland, OH 44026 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-09-10 |
| Decision Date | 2019-01-28 |
| Summary: | summary |