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KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

Page Type
Cleared 510(K)
510(k) Number
K013982
510(k) Type
Traditional
Applicant
Kinamed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2002
Days to Decision
169 days
Submission Type
Statement

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

Page Type
Cleared 510(K)
510(k) Number
K013982
510(k) Type
Traditional
Applicant
Kinamed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2002
Days to Decision
169 days
Submission Type
Statement