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HOWMEDICA PRECISION OSTEOLOCK FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K881983
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1988
Days to Decision
147 days

HOWMEDICA PRECISION OSTEOLOCK FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K881983
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1988
Days to Decision
147 days