STCC
Intervertebral Fusion Device With Bone Graft, Cervical
CARDINAL SPINE, LLC
The following data is part of a premarket notification filed by Cardinal Spine, Llc with the FDA for Stcc.
Pre-market Notification Details
| Device ID | K100698 |
| 510k Number | K100698 |
| Device Name: | STCC |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | CARDINAL SPINE, LLC 11234 EL CAMINO REAL, SUITE 200 San Diego, CA 9213 |
| Contact | David J Collette |
| Correspondent | David J Collette CARDINAL SPINE, LLC 11234 EL CAMINO REAL, SUITE 200 San Diego, CA 9213 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-03-11 |
| Decision Date | 2011-03-14 |
| Summary: | summary |
Trademark Results [STCC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 STCC 76306931 2784737 Dead/Cancelled |
STMicroelectronics, Inc. 2001-08-30 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.