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ARTHREX CHONDRAL DART, MODEL AR-4005B-18

Page Type
Cleared 510(K)
510(k) Number
K991971
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2000
Days to Decision
420 days
Submission Type
Summary

ARTHREX CHONDRAL DART, MODEL AR-4005B-18

Page Type
Cleared 510(K)
510(k) Number
K991971
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2000
Days to Decision
420 days
Submission Type
Summary