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RINGLOC 36MM LINE AND MODULAR FEMORAL HEADS

Page Type
Cleared 510(K)
510(k) Number
K032396
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2003
Days to Decision
17 days
Submission Type
Summary

RINGLOC 36MM LINE AND MODULAR FEMORAL HEADS

Page Type
Cleared 510(K)
510(k) Number
K032396
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2003
Days to Decision
17 days
Submission Type
Summary