| Record ID | N16837 |
|---|---|
| Device Name | ARTEGRAFT{TM} AND REINFORCED ARTEGRAFT{TM} |
| Applicant | LeMaitre Vascular, Inc. |
| Product Code | LXA · Cardiovascular |
| Decision Date | Aug 1, 1979 |
| Decision | APPR |
| Device Class | Class 3 |
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