Biomet Orthopedics, Inc. · Class II · Cleared May 31, 2002
| K-number | K021403 |
| Device name | HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM |
| Applicant | Biomet Orthopedics, Inc. |
| Product code | MEH |
| Device class | Class II |
| Decision date | May 31, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 888.3353 |
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