The following data is part of a premarket notification filed by Institut Straumann Ag with the FDA for Straumann Wn Cares Titanium Abutment.
Device ID | K082764 |
510k Number | K082764 |
Device Name: | STRAUMANN WN CARES TITANIUM ABUTMENT |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | INSTITUT STRAUMANN AG 60 MINUTEMAN ROAD Andover, MA 01810 |
Contact | Elaine Alan |
Correspondent | Elaine Alan INSTITUT STRAUMANN AG 60 MINUTEMAN ROAD Andover, MA 01810 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-09-22 |
Decision Date | 2008-10-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
07630031717788 | K082764 | 000 |