FDA 510(k) Applications Submitted by CRESCO TI SYSTEMS AB

FDA 510(k) Number Submission Date Device Name Applicant
K042354 08/30/2004 MODIFICATION TO: CRESCO TI IMPLANT CONCEPT CRESCO TI SYSTEMS AB
K981052 03/23/1998 CRESCO TI IMPLANT CONCEPT CRESCO TI SYSTEMS AB


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