The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Vertex Reconstruction System.
Device ID | K083071 |
510k Number | K083071 |
Device Name: | VERTEX RECONSTRUCTION SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 -3576 |
Contact | Melisa Lansky |
Correspondent | Melisa Lansky MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 -3576 |
Product Code | KWP |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-10-15 |
Decision Date | 2008-11-14 |
Summary: | summary |