The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive Peek Corpectomy Railed System.
Device ID | K151538 |
510k Number | K151538 |
Device Name: | NuVasive PEEK Corpectomy Railed System |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Contact | Olga Lewis |
Correspondent | Olga Lewis NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-08 |
Decision Date | 2015-09-04 |
Summary: | summary |