The following data is part of a premarket notification filed by Sofamor Danek Usa,inc. with the FDA for Cd Horizon Spinal System.
| Device ID | K981676 | 
| 510k Number | K981676 | 
| Device Name: | CD HORIZON SPINAL SYSTEM | 
| Classification | Appliance, Fixation, Spinal Interlaminal | 
| Applicant | SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 | 
| Contact | Richard W Treharne | 
| Correspondent | Richard W Treharne SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 | 
| Product Code | KWP | 
| Subsequent Product Code | KWQ | 
| Subsequent Product Code | MNH | 
| Subsequent Product Code | MNI | 
| CFR Regulation Number | 888.3050 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 1998-05-12 | 
| Decision Date | 1999-01-28 | 
| Summary: | summary |