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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