Howmedica, Pfizer Medical Technology Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Howmedica, Pfizer Medical Technology Group - FDA 510(k) Cleared Devic...
1
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Cleared
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Denied
Howmedica, Pfizer Medical Technology Group has 1 FDA 510(k) cleared medical devices. Based in Rutherford, US.
Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Howmedica, Pfizer Medical Technology Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Howmedica, Pfizer Medical Technology Group
1 devices