The following data is part of a premarket notification filed by Nuvasive, Inc. with the FDA for Brigade Standalone System.
Device ID | K123045 |
510k Number | K123045 |
Device Name: | BRIGADE STANDALONE SYSTEM |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
Contact | Cynthia Adams |
Correspondent | Cynthia Adams NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-10-01 |
Decision Date | 2013-04-16 |
Summary: | summary |