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ARTHROTEK SET SCREW

Page Type
Cleared 510(K)
510(k) Number
K932721
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/1/1994
Days to Decision
423 days
Submission Type
Summary

ARTHROTEK SET SCREW

Page Type
Cleared 510(K)
510(k) Number
K932721
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/1/1994
Days to Decision
423 days
Submission Type
Summary