The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Modification To Vertex Reconstruction System.
| Device ID | K080805 |
| 510k Number | K080805 |
| Device Name: | MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
| Contact | Christine Scifert |
| Correspondent | Christine Scifert MEDTRONIC SOFAMOR DANEK 1800 PYRAMID PLACE Memphis, TN 38132 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-03-21 |
| Decision Date | 2008-04-18 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00613994362018 | K080805 | 000 |
| 00613994362001 | K080805 | 000 |
| 00613994239242 | K080805 | 000 |
| 00613994239235 | K080805 | 000 |
| 00613994239228 | K080805 | 000 |
| 00613994239211 | K080805 | 000 |