The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Malibu Spinal System With The Daytona Deformity System.
Device ID | K122571 |
510k Number | K122571 |
Device Name: | MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | SEASPINE, INC. 2302 La Mirada Dr Vista, CA 92081 |
Contact | Ethel Bernal |
Correspondent | Ethel Bernal SEASPINE, INC. 2302 La Mirada Dr Vista, CA 92081 |
Product Code | NKB |
Subsequent Product Code | KWP |
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 | 2012-08-23 |
Decision Date | 2012-12-12 |
Summary: | summary |