The following data is part of a premarket notification filed by Cardinal Spine, Llc with the FDA for Stgc.
| Device ID | K121176 |
| 510k Number | K121176 |
| Device Name: | STGC |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | CARDINAL SPINE, LLC 11234 EL CAMINO REAL, SUITE 200 San Diego, CA 9213 |
| Contact | Kevin A Thomas |
| Correspondent | Kevin A Thomas CARDINAL SPINE, LLC 11234 EL CAMINO REAL, SUITE 200 San Diego, CA 9213 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-18 |
| Decision Date | 2012-08-17 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() STGC 75516629 not registered Dead/Abandoned |
Startec Global Communications Corporation 1998-07-10 |