The following data is part of a premarket notification filed by Nuvasive, Inc. with the FDA for Nuvasive Smartplate Gradient Plus System.
Device ID | K053581 |
510k Number | K053581 |
Device Name: | NUVASIVE SMARTPLATE GRADIENT PLUS SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | NUVASIVE, INC. 4545 TOWNE CENTRE COURT San Diego, CA 92121 |
Contact | Laetitia Cousin |
Correspondent | Laetitia Cousin NUVASIVE, INC. 4545 TOWNE CENTRE COURT San Diego, CA 92121 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-12-23 |
Decision Date | 2006-02-17 |
Summary: | summary |