The following data is part of a premarket notification filed by Dentsply International, Inc. with the FDA for Quattro Porcelain System.
| Device ID | K091706 |
| 510k Number | K091706 |
| Device Name: | QUATTRO PORCELAIN SYSTEM |
| Classification | Powder, Porcelain |
| Applicant | DENTSPLY INTERNATIONAL, INC. 221 WEST PHILADELPHIA ST. SUITE 60 York, PA 17404 |
| Contact | Helen Lewis |
| Correspondent | Helen Lewis DENTSPLY INTERNATIONAL, INC. 221 WEST PHILADELPHIA ST. SUITE 60 York, PA 17404 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-06-10 |
| Decision Date | 2009-08-28 |
| Summary: | summary |