Bioplate, Inc. · Class II · Cleared Oct 5, 2000
| K-number | K002879 |
| Device name | MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM |
| Applicant | Bioplate, Inc. |
| Product code | JEY |
| Device class | Class II |
| Decision date | Oct 5, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 872.4760 |
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