K061981 is an FDA 510(k) clearance for the SURPASS. This device is classified as a Agent, Tooth Bonding, Resin (Class II - Special Controls, product code KLE).
Submitted by Apex Dental Materials, Inc. (Deer Park, US). The FDA issued a Cleared decision on July 31, 2006, 18 days after receiving the submission on July 13, 2006.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3200.
| 510(k) Number | K061981 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 13, 2006 |
| Decision Date | July 31, 2006 |
| Days to Decision | 18 days |
| Submission Type | Abbreviated |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | KLE - Agent, Tooth Bonding, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3200 |