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ARTHREX MENISCAL DART SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983577
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1999
Days to Decision
304 days
Submission Type
Summary

ARTHREX MENISCAL DART SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K983577
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1999
Days to Decision
304 days
Submission Type
Summary