The following data is part of a premarket notification filed by Nobel Biocare Ab with the FDA for Nobelprocera Ti Abutment Thommen Platforms.
| Device ID | K101714 |
| 510k Number | K101714 |
| Device Name: | NOBELPROCERA TI ABUTMENT THOMMEN PLATFORMS |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | NOBEL BIOCARE AB 22715 SAVI RANCH PKWY. Yorba Linda, CA 92887 |
| Contact | Herbert Crane |
| Correspondent | Herbert Crane NOBEL BIOCARE AB 22715 SAVI RANCH PKWY. Yorba Linda, CA 92887 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-06-18 |
| Decision Date | 2010-08-31 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07332747101126 | K101714 | 000 |
| 07332747013788 | K101714 | 000 |
| 07332747101034 | K101714 | 000 |
| 07332747101041 | K101714 | 000 |
| 07332747101058 | K101714 | 000 |
| 07332747101065 | K101714 | 000 |
| 07332747101072 | K101714 | 000 |
| 07332747101089 | K101714 | 000 |
| 07332747101096 | K101714 | 000 |
| 07332747101102 | K101714 | 000 |
| 07332747101119 | K101714 | 000 |
| 07332747013771 | K101714 | 000 |