FDA 510(k) Applications Submitted by DEPUY MITEK, A JOHNSON & JOHNSON CO.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082282 | 08/11/2008 | HEALIX TI ANCHOR | DEPUY MITEK, A JOHNSON & JOHNSON CO. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact