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 |