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ARTHREX TIBIAL TUNNEL CANNULA

Page Type
Cleared 510(K)
510(k) Number
K930152
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1994
Days to Decision
423 days
Submission Type
Statement

ARTHREX TIBIAL TUNNEL CANNULA

Page Type
Cleared 510(K)
510(k) Number
K930152
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1994
Days to Decision
423 days
Submission Type
Statement