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SECOND GENERATION KNEE SYSTEM, FEMORAL, PATELLAR

Page Type
Cleared 510(K)
510(k) Number
K895145
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/6/1990
Days to Decision
322 days

SECOND GENERATION KNEE SYSTEM, FEMORAL, PATELLAR

Page Type
Cleared 510(K)
510(k) Number
K895145
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/6/1990
Days to Decision
322 days