The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Seaspine Spacer System - (hollywood, Pacifica, Redondo, Ventura) Nanometalene, Cambria Nanometalene , Vu Apod-l Nanometalene, Vu Epod Nanometalene.
| Device ID | K142488 |
| 510k Number | K142488 |
| Device Name: | SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu APOD-L NanoMetalene, Vu EPOD NanoMetalene |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | SeaSpine, Inc. 2302 La Mirada Drive Vista, CA 92081 |
| Contact | Michelle Willis |
| Correspondent | Michelle Willis SeaSpine, Inc. 2302 La Mirada Drive Vista, CA 92081 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-04 |
| Decision Date | 2014-12-18 |
| Summary: | summary |