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ARCOMXL POLYETHYLENE LINERS AND 38/40MM FEMORAL HEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062997
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
67 days
Submission Type
Summary

ARCOMXL POLYETHYLENE LINERS AND 38/40MM FEMORAL HEADS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062997
510(k) Type
Traditional
Applicant
Biomet Manufacturing Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2006
Days to Decision
67 days
Submission Type
Summary