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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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