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News   FDA

Minnesota Medical Development, Inc.'s Hernia Device Gains Clearance from FDA

October 5, 2007 | 
1 min read
Minnesota Medical Development, Inc. (MMDI) reports that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance to its new Rebound Hernia Repair Device (HRT).
FDA Approvals
Food and Drug Administration (FDA)
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