Protek, Inc. · Class II · Cleared Dec 29, 1988
| K-number | K884888 |
| Device name | MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS |
| Applicant | Protek, Inc. |
| Product code | JDI |
| Device class | Class II |
| Decision date | Dec 29, 1988 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 888.3350 |
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