The following data is part of a premarket notification filed by Thommen Medical, Ag with the FDA for Spi Variomulti Abutment.
| Device ID | K072856 |
| 510k Number | K072856 |
| Device Name: | SPI VARIOMULTI ABUTMENT |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | THOMMEN MEDICAL, AG 11234 EL CAMINO REAL, STE. 200 San Diego, CA 92130 |
| Contact | Linda K Schulz |
| Correspondent | Linda K Schulz THOMMEN MEDICAL, AG 11234 EL CAMINO REAL, STE. 200 San Diego, CA 92130 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-05 |
| Decision Date | 2008-02-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07640156476149 | K072856 | 000 |
| 07640156472974 | K072856 | 000 |
| 07640156473254 | K072856 | 000 |
| 07640156473261 | K072856 | 000 |
| 07640156473278 | K072856 | 000 |
| 07640156473285 | K072856 | 000 |
| 07640156473292 | K072856 | 000 |
| 07640156473308 | K072856 | 000 |
| 07640156473315 | K072856 | 000 |
| 07640156473322 | K072856 | 000 |
| 07640156473339 | K072856 | 000 |
| 07640156473346 | K072856 | 000 |
| 07640156473353 | K072856 | 000 |
| 07640156473360 | K072856 | 000 |
| 07640156473674 | K072856 | 000 |
| 07640156474145 | K072856 | 000 |
| 07640156472165 | K072856 | 000 |