| K-number | K911768 |
| Device name | AMSET(TM) BONE SCREW |
| Applicant | Advanced Med/Surg, Inc. |
| Product code | HWC |
| Device class | Class II |
| Decision date | Oct 4, 1991 |
| 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