The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Crescent (r) Spinal System Titanium.
Device ID | K110543 |
510k Number | K110543 |
Device Name: | CRESCENT (R) SPINAL SYSTEM TITANIUM |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Becky Ronner |
Correspondent | Becky Ronner MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-02-25 |
Decision Date | 2011-08-09 |
Summary: | summary |