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CEMENTED FEMORAL HEAD RESURFING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021799
510(k) Type
Special
Applicant
Biomet Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2002
Days to Decision
26 days
Submission Type
Summary

CEMENTED FEMORAL HEAD RESURFING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021799
510(k) Type
Special
Applicant
Biomet Orthopedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2002
Days to Decision
26 days
Submission Type
Summary