FDA 510(k), K150669, Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)

510(K) Number: K150669
Device Name: Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)
Manufacturer: Karin Darle Olsson
Device Classification Name: Abutment, Implant, Dental, Endosseous
Regulation Number: NHA
Classification Product Code: 03/16/2015
Date Received: 10/08/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental

Number of Pages: 365 (out of 455 were unredacted)