| K-number | K903362 |
| Device name | OSTEOLOCK(TM) ACETABULAR CUP |
| Applicant | Howmedica Corp. |
| Product code | JDI |
| Device class | Class II |
| Decision date | Oct 22, 1990 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 888.3350 |
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