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 |