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PRECISION OSTEOFLEX FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K903630
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1994
Days to Decision
1293 days

PRECISION OSTEOFLEX FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K903630
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1994
Days to Decision
1293 days