Howmedica Corp. · Class II · Cleared Sep 1, 1994
| K-number | K930275 |
| Device name | PRECISION OSTEOLOCK ACETABULAR COMPONENT |
| Applicant | Howmedica Corp. |
| Product code | JDI |
| Device class | Class II |
| Decision date | Sep 1, 1994 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 888.3350 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov