The following data is part of a premarket notification filed by Altatec Gmbh with the FDA for Camlog Dental Implant Abutments, Healing Caps, And Accessories.
| Device ID | K051636 |
| 510k Number | K051636 |
| Device Name: | CAMLOG DENTAL IMPLANT ABUTMENTS, HEALING CAPS, AND ACCESSORIES |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | ALTATEC GMBH 520 SOUTH ROCK BLVD. Reno, NV 89502 |
| Contact | Tina Steffanie-oak |
| Correspondent | Tina Steffanie-oak ALTATEC GMBH 520 SOUTH ROCK BLVD. Reno, NV 89502 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-06-20 |
| Decision Date | 2006-02-17 |
| Summary: | summary |