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ANSPACH MENISECTOMY KNIFE

Page Type
Cleared 510(K)
510(k) Number
K803178
510(k) Type
Traditional
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1981
Days to Decision
59 days

ANSPACH MENISECTOMY KNIFE

Page Type
Cleared 510(K)
510(k) Number
K803178
510(k) Type
Traditional
Applicant
THE ANSPACH EFFORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1981
Days to Decision
59 days