Codman & Shurtleff, Inc. · Class II · Cleared Feb 25, 2004
| K-number | K033395 |
| Device name | CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1 |
| Applicant | Codman & Shurtleff, Inc. |
| Product code | GXO |
| Device class | Class II |
| Decision date | Feb 25, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 882.5900 |
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