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RESORBABLE SCREW ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K012872
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
85 days
Submission Type
Summary

RESORBABLE SCREW ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K012872
510(k) Type
Traditional
Applicant
ARTHROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2001
Days to Decision
85 days
Submission Type
Summary