The following data is part of a premarket notification filed by Altatec Gmbh with the FDA for Camlog Logfit Prosthetic System.
| Device ID | K071213 |
| 510k Number | K071213 |
| Device Name: | CAMLOG LOGFIT PROSTHETIC SYSTEM |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | ALTATEC GMBH 11234 EL CAMINO REAL SUITE 200 San Diego, CA 92130 |
| Contact | Floyd G Larson |
| Correspondent | Floyd G Larson ALTATEC GMBH 11234 EL CAMINO REAL SUITE 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 | 2007-05-01 |
| Decision Date | 2007-08-10 |
| Summary: | summary |