Integra LifeSciences Corporation · Class II · Cleared Jan 21, 2010
| K-number | K092388 |
| Device name | DURAGEN PLUS DURAL REGENERATION MATRIX- SPINAL MATRIX, MODEL DP2013SM, INTEGRA SPINAL MEND DURAL REGENERATION MATRIX, MO |
| Applicant | Integra LifeSciences Corporation |
| Product code | GXQ |
| Device class | Class II |
| Decision date | Jan 21, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 882.5910 |
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