FDA 510(k), K842493, AGEE EXTERNAL FIXATOR
FDA 510(k), K842493, AGEE EXTERNAL FIXATOR
Device Name: AGEE EXTERNAL FIXATOR
Manufacturer:
Device Classification Name: Component, Traction, Invasive
Regulation Number: JEC
Classification Product Code: KXA
Date Received: 06/26/1984
Decision Date: 02/13/1985
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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