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ARTHREX SUTURE GRAFTING KIT

Page Type
Cleared 510(K)
510(k) Number
K041553
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
184 days
Submission Type
Summary

ARTHREX SUTURE GRAFTING KIT

Page Type
Cleared 510(K)
510(k) Number
K041553
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2004
Days to Decision
184 days
Submission Type
Summary