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MENISCAL CINCH

Page Type
Cleared 510(K)
510(k) Number
K073149
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2008
Days to Decision
95 days
Submission Type
Summary

MENISCAL CINCH

Page Type
Cleared 510(K)
510(k) Number
K073149
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2008
Days to Decision
95 days
Submission Type
Summary