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ARTHREX ARTHOERESIS IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K053543
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2006
Days to Decision
104 days
Submission Type
Summary

ARTHREX ARTHOERESIS IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K053543
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2006
Days to Decision
104 days
Submission Type
Summary