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NAVIPRO KNEE SOFTWARE MODULE

Page Type
Cleared 510(K)
510(k) Number
K033668
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2004
Days to Decision
111 days
Submission Type
Summary

NAVIPRO KNEE SOFTWARE MODULE

Page Type
Cleared 510(K)
510(k) Number
K033668
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2004
Days to Decision
111 days
Submission Type
Summary