FDA 510(k) Applications Submitted by HOOGLAND SPINE PRODUCTS GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K090132 01/21/2009 MAXMORESPINE SPINAL SYSTEM HOOGLAND SPINE PRODUCTS GMBH
K083552 12/01/2008 MAXMORESPINE TOM STICK HOOGLAND SPINE PRODUCTS GMBH


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