The following data is part of a premarket notification filed by Seaspine, Inc. with the FDA for Sierra.
| Device ID | K062934 |
| 510k Number | K062934 |
| Device Name: | SIERRA |
| Classification | Orthosis, Spinal Pedicle Fixation |
| Applicant | SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
| Contact | Diana Smith |
| Correspondent | Diana Smith SEASPINE, INC. 2302 LA MIRADA DR. Vista, CA 92081 -7862 |
| Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-09-28 |
| Decision Date | 2006-11-16 |
| Summary: | summary |