The following data is part of a premarket notification filed by Straumann Usa with the FDA for Straumann Rc Temporary Abutments.
| Device ID | K093027 |
| 510k Number | K093027 |
| Device Name: | STRAUMANN RC TEMPORARY ABUTMENTS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | STRAUMANN USA 60 MINUTEMAN ROAD Andover, MA 01810 |
| Contact | Elaine Alan |
| Correspondent | Elaine Alan STRAUMANN USA 60 MINUTEMAN ROAD Andover, MA 01810 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-29 |
| Decision Date | 2010-02-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07630031710918 | K093027 | 000 |
| 07630031710895 | K093027 | 000 |