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CERVICAL SPATULA

Page Type
Cleared 510(K)
510(k) Number
K811548
510(k) Type
Traditional
Applicant
PROCEDURE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1981
Days to Decision
22 days

CERVICAL SPATULA

Page Type
Cleared 510(K)
510(k) Number
K811548
510(k) Type
Traditional
Applicant
PROCEDURE PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1981
Days to Decision
22 days