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 |