Aesculap, Inc. · Class II · Cleared Aug 15, 1994
| K-number | K936269 |
| Device name | CASPAR TITANIUM ALLOY BONE SCREWS |
| Applicant | Aesculap, Inc. |
| Product code | KWQ |
| Device class | Class II |
| Decision date | Aug 15, 1994 |
| Decision | Substantially Equivalent for Some Indications |
| 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