FDA 510(k) Applications Submitted by CAROL CHANG

FDA 510(k) Number Submission Date Device Name Applicant
K090839 03/27/2009 MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS SYNTEC SCIENTIFIC CORP.
K101971 07/13/2010 SYNTEC OS SPINAL FIXATION SYSTEM SYNTEC SCIENTIFIC CORP.
K092889 09/21/2009 SYNTEC OSTEO-PLATE AND SCREW FIXATION SYNTEC SCIENTIFIC CORP.


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