FDA 510(k) Applications Submitted by MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101363 | 05/14/2010 | VU CPOD INTERVERTEBRAL BODU FUSION DEVICE | MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact