Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Minnesota Medical Development, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K083467 REBOUND HRDVFTL2009-04-23 View
510(k) K080393 MODIFICATION TO REBOUND HRDFTL2008-03-13 View
510(k) K063671 REBOUND HRDFTL2007-08-16 View
↑