The following data is part of a premarket notification filed by Straumann Usa with the FDA for Straumann Computer Aided Restoration Service.
| Device ID | K052272 |
| 510k Number | K052272 |
| Device Name: | STRAUMANN COMPUTER AIDED RESTORATION SERVICE |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | STRAUMANN USA 60 MINUTETEMAN ROAD Andover, MA 01810 |
| Contact | Elaine Alan |
| Correspondent | Elaine Alan STRAUMANN USA 60 MINUTETEMAN 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 | 2005-08-22 |
| Decision Date | 2006-01-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07630031728623 | K052272 | 000 |
| 07630031717764 | K052272 | 000 |