| K-number | K964252 |
| Device name | ORTHOCHUCK |
| Applicant | Buckman Co., Inc. |
| Product code | GEY |
| Device class | Class I |
| Decision date | May 27, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 878.4820 |
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