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PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA

Page Type
Cleared 510(K)
510(k) Number
K896853
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/2/1990
Days to Decision
148 days

PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA

Page Type
Cleared 510(K)
510(k) Number
K896853
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/2/1990
Days to Decision
148 days