The following data is part of a premarket notification filed by Sterngold with the FDA for Sterngold 3.25 Era Dental Implant System.
Device ID | K041271 |
510k Number | K041271 |
Device Name: | STERNGOLD 3.25 ERA DENTAL IMPLANT SYSTEM |
Classification | Implant, Endosseous, Root-form |
Applicant | STERNGOLD 5 WHITCOMB AVE. Ayer, MA 01432 |
Contact | Pamela Papineau |
Correspondent | Pamela Papineau STERNGOLD 5 WHITCOMB AVE. Ayer, MA 01432 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-12 |
Decision Date | 2004-10-28 |
Summary: | summary |