FDA 510(k) Applications Submitted by SULZER MEDICA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K992832 | 08/23/1999 | SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS | SULZER MEDICA |
| K993667 | 11/01/1999 | SULZER VASCUTEK SEALPTFE VASCULAR PROSTHESIS | SULZER MEDICA |
| K002324 | 07/31/2000 | MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA | SULZER MEDICA |
| K993569 | 10/21/1999 | APR METASUL ACETABULAR INSERT | SULZER MEDICA |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact