KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT— 510(k) K013982

Substantially Equivalent

Kinamed, Inc.

FDA 510(k) clearance K013982 for KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT, Substantially Equivalent on 2002-05-21. Applicant: Kinamed, Inc..

Clearance details

Applicant: Kinamed, Inc.
Product code: Code KRR
Advisory panel: Orthopedic
Date received: 2001-12-03
Decision date: 2002-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

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