Aesculap, Inc. · Class II · Cleared Dec 9, 1997
| K-number | K970851 |
| Device name | LYOPLANT DURA SUBSTITUTE(VARIOUS) |
| Applicant | Aesculap, Inc. |
| Product code | GXQ |
| Device class | Class II |
| Decision date | Dec 9, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 882.5910 |
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