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MODULAR PROTUSIO CUP

Page Type
Cleared 510(K)
510(k) Number
K990032
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1999
Days to Decision
43 days
Submission Type
Summary

MODULAR PROTUSIO CUP

Page Type
Cleared 510(K)
510(k) Number
K990032
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1999
Days to Decision
43 days
Submission Type
Summary