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PORTLAND COBALT CHROME FEMORAL HEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063278
510(k) Type
Traditional
Applicant
Portland Orthopaedics Limited
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2007
Days to Decision
73 days
Submission Type
Summary

PORTLAND COBALT CHROME FEMORAL HEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063278
510(k) Type
Traditional
Applicant
Portland Orthopaedics Limited
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2007
Days to Decision
73 days
Submission Type
Summary