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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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