FDA 510(k), K033769, EIUS UNICOMPARTMENTAL KNEE SYSTEM

FDA 510(k), K033769, EIUS UNICOMPARTMENTAL KNEE SYSTEM

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510(K) Number: K033769
Device Name: EIUS UNICOMPARTMENTAL KNEE SYSTEM
Manufacturer:
Device Classification Name: Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Regulation Number: 888.3520
Classification Product Code: HSX
Date Received: 12/03/2003
Decision Date: 02/13/2004
Regulation Medical Specialty: Orthopedic
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