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 |