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FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892059
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1989
Days to Decision
112 days

FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892059
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/1989
Days to Decision
112 days