Regeneration Technologies, Inc. · Class II · Cleared Oct 24, 2007
| K-number | K072327 |
| Device name | CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON |
| Applicant | Regeneration Technologies, Inc. |
| Product code | MQV |
| Device class | Class II |
| Decision date | Oct 24, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 888.3045 |
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