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.

Danek Group, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K936307 DYNA-LOK ANTERIOR PLATING SYSTEMMNH1995-08-14 View
510(k) K934582 GDLH VARIABLE ANGLE CONNECTORKWP1994-06-21 View
↑