The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for T2 Xvbr 1.5 Spinal System.
Device ID | K100976 |
510k Number | K100976 |
Device Name: | T2 XVBR 1.5 SPINAL SYSTEM |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Theresa Leister |
Correspondent | Theresa Leister MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-04-08 |
Decision Date | 2010-10-21 |
Summary: | summary |