The following data is part of a premarket notification filed by Prismatik Dentalcraft, Inc. with the FDA for Inclusive Titanium Abutments For Camlog Screw-line Implants.
Device ID | K121391 |
510k Number | K121391 |
Device Name: | INCLUSIVE TITANIUM ABUTMENTS FOR CAMLOG SCREW-LINE IMPLANTS |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | PRISMATIK DENTALCRAFT, INC. 2212 DUPONT DR., ST P Irvine, CA 92612 |
Contact | Armin Zehtabchi |
Correspondent | Armin Zehtabchi PRISMATIK DENTALCRAFT, INC. 2212 DUPONT DR., ST P Irvine, CA 92612 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-05-09 |
Decision Date | 2012-12-10 |
Summary: | summary |