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FDA 510(k) Applications Submitted by KLASS BESSELING
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062834
09/21/2006
OSTEON, MODELS GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050
GENOSS CO., LTD.
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