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CEMENT, ULTRA-BOND

Page Type
Cleared 510(K)
510(k) Number
K760239
510(k) Type
Traditional
Applicant
ORATEC DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1976
Days to Decision
11 days

CEMENT, ULTRA-BOND

Page Type
Cleared 510(K)
510(k) Number
K760239
510(k) Type
Traditional
Applicant
ORATEC DENTAL PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/1976
Days to Decision
11 days