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 |