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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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