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ARTHREX BIO-PIN

Page Type
Cleared 510(K)
510(k) Number
K050259
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
113 days
Submission Type
Summary

ARTHREX BIO-PIN

Page Type
Cleared 510(K)
510(k) Number
K050259
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2005
Days to Decision
113 days
Submission Type
Summary