FDA 510(k) Applications Submitted by IMZ, GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K963495 09/03/1996 IMZ 2000 INTERLOCK 12/3 - CYLINDER DENTAL IMPLANT SYSTEM IMZ, GMBH
K963520 09/03/1996 IMZ TWIN PLUS SCREW IMZ, GMBH
K963521 09/03/1996 IMZ TWIN PLUS - CYLINDER IMZ, GMBH
K963522 09/03/1996 IMZ 2000 INTERLOCK 12/3 - SCREW IMZ, GMBH


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