FDA 510(k) Applications Submitted by LANNY J JOHNSON

FDA 510(k) Number Submission Date Device Name Applicant
K980999 03/18/1998 ST LEGER CEMENTED SEMI-CONSTRAINED TOTAL KNEE IMPLANT INSTRUMENT MAKAR, INC.
K002600 08/21/2000 LITWIN CRUICATE ANCHOR INSTRUMENT MAKAR, INC.


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