The following data is part of a premarket notification filed by Depuy Spine, Inc. with the FDA for Summit Oct Spinal System.
Device ID | K041203 |
510k Number | K041203 |
Device Name: | SUMMIT OCT SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | DEPUY SPINE, INC. 325 PARAMOUNT DR. Raynham, MA 02767 |
Contact | Sharon Starowicz |
Correspondent | Sharon Starowicz DEPUY SPINE, INC. 325 PARAMOUNT DR. Raynham, MA 02767 |
Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-07 |
Decision Date | 2004-06-02 |
Summary: | summary |