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Portland Orthopaedics Pty. , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061564PORTLAND CERAMIC (BIOLOX-FORTE) FEMORAL HEADSeptember 1, 2006
K053417M-COR HIP REPLACEMENT SYSTEMJuly 20, 2006
K051844EQUATOR PLUS ACETABULAR CUP SYSTEMOctober 7, 2005
K032641MODIFICATION TO: THE MARGRON HIP REPLACEMENT SYSTEMJanuary 20, 2004
K992815THE MARGRON HIP REPLACEMENT SYSTEMFebruary 7, 2000