K063718 is an FDA 510(k) clearance for the SFB AND CFB IMPLANTS - 5.0 PLATFORM. This device is classified as a Implant, Endosseous, Root-form (Class II - Special Controls, product code DZE).
Submitted by Nobel Biocare AB (Yorba Linda,, US). The FDA issued a Cleared decision on January 5, 2007, 22 days after receiving the submission on December 14, 2006.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3640.
| 510(k) Number | K063718 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 14, 2006 |
| Decision Date | January 05, 2007 |
| Days to Decision | 22 days |
| Submission Type | Special |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | DZE — Implant, Endosseous, Root-form |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3640 |