FDA 510(k) Applications Submitted by THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980534 | 02/11/1998 | DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608H | THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG |
| K960356 | 01/25/1996 | POSTERIOR ANNULOPLASTY BAND (MODEL 607) | THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact