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APR COLLARED REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885192
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/22/1989
Days to Decision
188 days

APR COLLARED REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885192
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/22/1989
Days to Decision
188 days