The following data is part of a premarket notification filed by Nuvasive, Inc. with the FDA for Nuvasive Polyaxial Spinal Screws.
Device ID | K121619 |
510k Number | K121619 |
Device Name: | NUVASIVE POLYAXIAL SPINAL SCREWS |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
Contact | Elias Ketchum |
Correspondent | Elias Ketchum NUVASIVE, INC. 7475 LUSK BLVD San Diego, CA 92121 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-06-01 |
Decision Date | 2012-08-24 |
Summary: | summary |