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REGENEREX TIBIAL COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K080361
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2008
Days to Decision
70 days
Submission Type
Summary

REGENEREX TIBIAL COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K080361
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/21/2008
Days to Decision
70 days
Submission Type
Summary