The following data is part of a premarket notification filed by Dentsply Intl. with the FDA for Orion E Alloy.
Device ID | K032316 |
510k Number | K032316 |
Device Name: | ORION E ALLOY |
Classification | Alloy, Gold-based Noble Metal |
Applicant | DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Contact | P. Jeffery Lehn |
Correspondent | P. Jeffery Lehn DENTSPLY INTL. 570 WEST COLLEGE AVE. P.O. BOX 872 York, PA 17405 |
Product Code | EJT |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-07-28 |
Decision Date | 2003-09-30 |
Summary: | summary |