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DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915512
510(k) Type
Traditional
Applicant
PFIZER HOSPITAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/18/1992
Days to Decision
253 days
Submission Type
Summary

DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915512
510(k) Type
Traditional
Applicant
PFIZER HOSPITAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/18/1992
Days to Decision
253 days
Submission Type
Summary