Osteo Technology, Inc. · Class II · Cleared Mar 9, 1994
| K-number | K926156 |
| Device name | REPLICA(TM) TOTAL HIP SYSTEM |
| Applicant | Osteo Technology, Inc. |
| Product code | LPH |
| Device class | Class II |
| Decision date | Mar 9, 1994 |
| Decision | Substantially Equivalent for Some Indications |
| Regulation | 888.3358 |
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