The following data is part of a premarket notification filed by Ortho Development with the FDA for Vusion(r) Os.
| Device ID | K111965 |
| 510k Number | K111965 |
| Device Name: | VUSION(R) OS |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | ORTHO DEVELOPMENT 12187 S. BUSINESS PARK DR. Draper, UT 84020 |
| Contact | Tom Haueter |
| Correspondent | Tom Haueter ORTHO DEVELOPMENT 12187 S. BUSINESS PARK DR. Draper, UT 84020 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-07-11 |
| Decision Date | 2011-10-25 |
| Summary: | summary |