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KINAMED PROFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K964362
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1997
Days to Decision
76 days
Submission Type
Statement

KINAMED PROFIX SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K964362
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1997
Days to Decision
76 days
Submission Type
Statement