The following data is part of a premarket notification filed by Aalba Dent, Inc. with the FDA for Platalloy.
Device ID | K972607 |
510k Number | K972607 |
Device Name: | PLATALLOY |
Classification | Alloy, Metal, Base |
Applicant | AALBA DENT, INC. 400 WATT DR. Cordelia, CA 94534 |
Contact | Vincent M Benetti |
Correspondent | Vincent M Benetti AALBA DENT, INC. 400 WATT DR. Cordelia, CA 94534 |
Product Code | EJH |
CFR Regulation Number | 872.3710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-07-11 |
Decision Date | 1997-10-10 |