The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Clydesdale Spinal System.
| Device ID | K083026 | 
| 510k Number | K083026 | 
| Device Name: | CLYDESDALE SPINAL SYSTEM | 
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar | 
| Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 -3576 | 
| Contact | Lee Grant | 
| Correspondent | Lee Grant MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 -3576 | 
| Product Code | MAX | 
| CFR Regulation Number | 888.3080 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2008-10-10 | 
| Decision Date | 2008-12-29 | 
| Summary: | summary |