K172137 is an FDA 510(k) clearance for the PIEZOTOME CUBE. This device is classified as a Drill, Bone, Powered (Class II - Special Controls, product code DZI).
Submitted by Satelec - Acteon Group (Merignac, FR). The FDA issued a Cleared decision on May 3, 2018, 290 days after receiving the submission on July 17, 2017.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4120.
| 510(k) Number | K172137 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 17, 2017 |
| Decision Date | May 03, 2018 |
| Days to Decision | 290 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | DZI - Drill, Bone, Powered |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.4120 |