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ARTHROTEK CANNULA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K934401
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1994
Days to Decision
196 days
Submission Type
Summary

ARTHROTEK CANNULA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K934401
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1994
Days to Decision
196 days
Submission Type
Summary