Omni Surgical, L.P. · Class II · Cleared Apr 2, 2009
| K-number | K081770 |
| Device name | BLACK WIDOW ANTERIOR BUTTRESS PLATE |
| Applicant | Omni Surgical, L.P. |
| Product code | KWQ |
| Device class | Class II |
| Decision date | Apr 2, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 888.3060 |
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