The following data is part of a premarket notification filed by Medtronic Sofamor Danek, Inc. with the FDA for Vertex Reconstruction System.
Device ID | K003780 |
510k Number | K003780 |
Device Name: | VERTEX RECONSTRUCTION SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | MEDTRONIC SOFAMOR DANEK, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Richard W Treharne |
Correspondent | Richard W Treharne MEDTRONIC SOFAMOR DANEK, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | KWP |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-12-07 |
Decision Date | 2001-09-28 |
Summary: | summary |