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ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083707
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2009
Days to Decision
231 days
Submission Type
Summary

ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K083707
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/2009
Days to Decision
231 days
Submission Type
Summary