FDA 510(k), K771708, WORRELL PATELLA

510(K) Number: K771708
Device Name: WORRELL PATELLA
Manufacturer:
Device Classification Name: Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
Regulation Number: HTG
Classification Product Code: KXA
Date Received: 09/12/1977
Decision Date: 10/06/1977
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic

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