Submission Details
| 510(k) Number | K192033 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 30, 2019 |
| Decision Date | June 09, 2020 |
| Days to Decision | 315 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
K192033 is an FDA 510(k) clearance for the Contour P-Insert 90, Contour P-Insert 45, Contour P-Insert Tri Tip, Contour P-Insert WC Tip, Contour P-Insert Quad Tip, a Drill, Bone, Powered (Class II — Special Controls, product code DZI), submitted by Bennett Jacoby, Dds, Ms, Inc. (Kailua Kona, US). The FDA issued a Cleared decision on June 9, 2020, 315 days after receiving the submission on July 30, 2019. This device falls under the Dental review panel. Regulated under 21 CFR 872.4120.
| 510(k) Number | K192033 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 30, 2019 |
| Decision Date | June 09, 2020 |
| Days to Decision | 315 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 |