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KINEMAX PLUS MODULAR STABILIZER FEMORAL COMPONENT AND FEMORAL SPACERS

Page Type
Cleared 510(K)
510(k) Number
K963796
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/9/1996
Days to Decision
77 days

KINEMAX PLUS MODULAR STABILIZER FEMORAL COMPONENT AND FEMORAL SPACERS

Page Type
Cleared 510(K)
510(k) Number
K963796
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/9/1996
Days to Decision
77 days