The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Capstone Control Spinal System, Capstone Control Ptc Spinal System.
| Device ID | K171107 | 
| 510k Number | K171107 | 
| Device Name: | CAPSTONE CONTROL Spinal System, CAPSTONE CONTROL PTC Spinal System | 
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar | 
| Applicant | Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132 | 
| Contact | Julie Bassett | 
| Correspondent | Raphael Mcinnis Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132  | 
| Product Code | MAX | 
| CFR Regulation Number | 888.3080 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2017-04-14 | 
| Decision Date | 2017-09-26 | 
| Summary: | summary |