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 |