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SYNATOMIC REVISION FEMORAL PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K860594
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/14/1986
Days to Decision
23 days

SYNATOMIC REVISION FEMORAL PROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K860594
510(k) Type
Traditional
Applicant
DEPUY, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/14/1986
Days to Decision
23 days