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JACE MODEL K200 KNEE CPM DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K912537
510(k) Type
Traditional
Applicant
THERA KINETICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1991
Days to Decision
67 days
Submission Type
Statement

JACE MODEL K200 KNEE CPM DEVICE, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K912537
510(k) Type
Traditional
Applicant
THERA KINETICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1991
Days to Decision
67 days
Submission Type
Statement