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FDA 510(k) Applications Submitted by MICRON PRECISION ENGINEERING, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K022768
08/21/2002
AMT POLYAXIAL PEDICLE SCREW
MICRON PRECISION ENGINEERING, INC.
K002059
07/06/2000
AMT SPINAL SYSTEM
MICRON PRECISION ENGINEERING, INC.
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