ArthroCare Corporation · Class II · Cleared Apr 1, 2014
| K-number | K133606 |
| Device name | N8TIVE ACL ANATOMIC RECONSTRUCTION SYSTEM, N8TIVE ACL FEMORAL IMPLANT, N8TIVE ACL TIBIAL IMPLANT, VARIOUS CLASS I ANCILL |
| Applicant | ArthroCare Corporation |
| Product code | MBI |
| Device class | Class II |
| Decision date | Apr 1, 2014 |
| 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