The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive® Precept™ Spinal System.
Device ID | K171894 |
510k Number | K171894 |
Device Name: | NuVasive® Precept™ Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Contact | Marysa Loustalot |
Correspondent | Marysa E. Loustalot NuVasive, Incorporated 7475 Lusk Boulevard San Diego, CA 92121 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-26 |
Decision Date | 2017-09-28 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NUVASIVE 76298757 2818737 Live/Registered |
NUVASIVE, INC. 2001-08-10 |
![]() NUVASIVE 75822001 2541247 Live/Registered |
NUVASIVE, INC. 1999-10-13 |