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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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