Last synced on 9 May 2025 at 11:05 pm

PROFORM CEMENTED TITANIUM REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970194
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1997
Days to Decision
83 days
Submission Type
Statement

PROFORM CEMENTED TITANIUM REVISION FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970194
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1997
Days to Decision
83 days
Submission Type
Statement