FDA 510(k) Applications Submitted by HEINZ E WICK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K011208 | 04/19/2001 | BIOVER | BIOVER AG |
| K003045 | 09/29/2000 | HA-TI (HAND TITANIUM SCREW) IMPLANT | HATI DENTAL AG. |
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