The following data is part of a premarket notification filed by Institut Straumann Ag with the FDA for Straumann Modified Dental Abutment.
| Device ID | K091701 |
| 510k Number | K091701 |
| Device Name: | STRAUMANN MODIFIED DENTAL 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-06-10 |
| Decision Date | 2009-12-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07630031709295 | K091701 | 000 |
| 07630031709288 | K091701 | 000 |
| 07630031709271 | K091701 | 000 |
| 07630031709264 | K091701 | 000 |
| 07630031709257 | K091701 | 000 |
| 07630031709240 | K091701 | 000 |
| 07630031709233 | K091701 | 000 |
| 07630031709226 | K091701 | 000 |