FDA 510(k) Applications Submitted by MICHELLE M PERRY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960660 | 02/16/1996 | HEMISPHERE ACETABULAR CUP | ORTHO DEVELOPMENT CORP. |
| K961793 | 05/09/1996 | BI-LOC BIPOLAR CUP | ORTHO DEVELOPMENT CORP. |
| K962448 | 06/24/1996 | PRIMALOC CEMENTED HIP SYSTEM | ORTHO DEVELOPMENT CORP. |
| K953977 | 08/23/1995 | PRIMALOC CEMENTLESS HIP SYSTEM | ORTHO DEVELOPMENT CORP. |
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