The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa with the FDA for Cornerstone (r) Psr Cervical Fusion System.
Device ID | K111264 |
510k Number | K111264 |
Device Name: | CORNERSTONE (R) PSR CERVICAL FUSION SYSTEM |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | MEDTRONIC SOFAMOR DANEK USA 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Regina Holmes |
Correspondent | Regina Holmes MEDTRONIC SOFAMOR DANEK USA 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-05-04 |
Decision Date | 2011-10-12 |
Summary: | summary |