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PROWICK

Page Type
Cleared 510(K)
510(k) Number
K083007
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2009
Days to Decision
182 days
Submission Type
Summary

PROWICK

Page Type
Cleared 510(K)
510(k) Number
K083007
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2009
Days to Decision
182 days
Submission Type
Summary