Memometal Technologies · Class II · Cleared Nov 17, 2011
| K-number | K112197 |
| Device name | MEMOMETAL INTRA-MEDULLARY BONE FASTENER |
| Applicant | Memometal Technologies |
| Product code | HTY |
| Device class | Class II |
| Decision date | Nov 17, 2011 |
| Decision | Substantially Equivalent |
| Regulation | 888.3040 |
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