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FDA 510(k) Applications Submitted by ORTHOLUTION CO., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082838
09/26/2008
ORLUS MINI SCREW
ORTHOLUTION CO., LTD.
K052968
10/21/2005
MODIFICATION TO: ORLUS MINI SCREW
ORTHOLUTION CO., LTD.
K050568
03/04/2005
ORLUS MINI SCREW
ORTHOLUTION CO., LTD.
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