The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Malibu Spinal System.
Device ID | K051942 |
510k Number | K051942 |
Device Name: | MALIBU SPINAL SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | SEASPINE, INC. 2302 LA MIRADA DRIVE Vista, CA 92081 -7862 |
Contact | Diana Smith |
Correspondent | Diana Smith SEASPINE, INC. 2302 LA MIRADA DRIVE Vista, CA 92081 -7862 |
Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
Subsequent Product Code | NKB |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-07-15 |
Decision Date | 2005-07-27 |
Summary: | summary |