Orthomet, Inc. · Class I · Cleared Jun 18, 1990
| K-number | K902259 |
| Device name | AXIOM TOTAL KNEE SYSTEM, TIBIAL COMPONENT |
| Applicant | Orthomet, Inc. |
| Product code | JWX |
| Device class | Class I |
| Decision date | Jun 18, 1990 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 866.2660 |
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