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PLUS TOTAL KNEE SYST/PERI POST DESIGN TIBIAL COMP

Page Type
Cleared 510(K)
510(k) Number
K901936
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/3/1990
Days to Decision
64 days

PLUS TOTAL KNEE SYST/PERI POST DESIGN TIBIAL COMP

Page Type
Cleared 510(K)
510(k) Number
K901936
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/3/1990
Days to Decision
64 days