The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Integra Expandable Interverebral Body Fusion Device (ibd) System.
Device ID | K133418 |
510k Number | K133418 |
Device Name: | INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
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 | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-11-07 |
Decision Date | 2014-05-01 |
Summary: | summary |