The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Integra Laminoplasty System.
| Device ID | K130830 |
| 510k Number | K130830 |
| Device Name: | INTEGRA LAMINOPLASTY SYSTEM |
| Classification | Orthosis, Spine, Plate, Laminoplasty, Metal |
| Applicant | SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
| Contact | Jeff Brittan |
| Correspondent | Jeff Brittan SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
| Product Code | NQW |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-03-26 |
| Decision Date | 2013-05-09 |
| Summary: | summary |