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INTERLOK BIO-MODULAR HUMERAL STEMS

Page Type
Cleared 510(K)
510(k) Number
K032507
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2003
Days to Decision
22 days
Submission Type
Summary

INTERLOK BIO-MODULAR HUMERAL STEMS

Page Type
Cleared 510(K)
510(k) Number
K032507
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2003
Days to Decision
22 days
Submission Type
Summary