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 |