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SECOND GENERATION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K894334
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/6/1989
Days to Decision
84 days

SECOND GENERATION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K894334
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/6/1989
Days to Decision
84 days