FDA 510(k), K800800, PATELLAR COMPONENT FOR LUBINUS PATELLAR

510(K) Number: K800800
Device Name: PATELLAR COMPONENT FOR LUBINUS PATELLAR
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: KXA
Date Received: 04/10/1980
Decision Date: 04/21/1980
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic

Contents: 510K submission

32 pages