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 |