Biomet, Inc. · Class II · Cleared Feb 17, 2005
| K-number | K043100 |
| Device name | BIO-MODULAR SHOULDER SYSTEM WITH HYDROXYAPATITE (HA) COATED GLENOID COMPONENTS |
| Applicant | Biomet, Inc. |
| Product code | MBF |
| Device class | Class II |
| Decision date | Feb 17, 2005 |
| Decision | Substantially Equivalent |
| Regulation | 888.3670 |
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