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ARTHREX GRAFT HARVESTING KIT

Page Type
Cleared 510(K)
510(k) Number
K941285
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
242 days
Submission Type
Statement

ARTHREX GRAFT HARVESTING KIT

Page Type
Cleared 510(K)
510(k) Number
K941285
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1994
Days to Decision
242 days
Submission Type
Statement