FDA 510(k) Applications Submitted by PORTLAND ORTHOPAEDICS PTY. LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K032641 08/27/2003 MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEM PORTLAND ORTHOPAEDICS PTY. LTD.
K061564 06/05/2006 PORTLAND CERAMIC (BIOLOX-FORTE) FEMORAL HEAD PORTLAND ORTHOPAEDICS PTY. LTD.
K051844 07/07/2005 EQUATOR PLUS ACETABULAR CUP SYSTEM PORTLAND ORTHOPAEDICS PTY. LTD.
K053417 12/08/2005 M-COR HIP REPLACEMENT SYSTEM PORTLAND ORTHOPAEDICS PTY. LTD.
K992815 08/20/1999 THE MARGRON HIP REPLACEMENT SYSTEM PORTLAND ORTHOPAEDICS PTY. LTD.


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