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ARTHROSCOPY INSTRUMENT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K911205
510(k) Type
Traditional
Applicant
DAVOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1991
Days to Decision
90 days

ARTHROSCOPY INSTRUMENT CANNULA

Page Type
Cleared 510(K)
510(k) Number
K911205
510(k) Type
Traditional
Applicant
DAVOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/1991
Days to Decision
90 days