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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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