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DUET SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K020056
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
6/26/2002
Days to Decision
169 days
Submission Type
Summary

DUET SUTURE ANCHOR

Page Type
Cleared 510(K)
510(k) Number
K020056
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
6/26/2002
Days to Decision
169 days
Submission Type
Summary