Korean bone implant product passed through FDA's pre-marketing review.

Oscotech locally developed BBP, a dental bone implant material, in 1999 and obtained the approval of the U.S. FDA's 510K (Pre-marketing review notification), which was the 2nd event in passing through the U. S. FDA's review after the dental implant.

Oscotech said "The quality system of BBP was renovated to get FDA's approval during the past 3 years and we finally succeeded in obtaining the a...