RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE


Device Classification Name

prosthesis, knee, femorotibial, constrained, cemented, metal/polymer

510(k) Number K023667
Device Name RT-PLUS SOLUTION & RT-PLUS MODULAR SOLUTION KNEE
Original Applicant
PLUS ORTHOPEDICS
1001 oakwood blvd.
round rock, 
TX 
78681 -2700

Original Contact j.d. webb
Regulation Number 888.3510
Classification Product Code
KRO  
Date Received 10/31/2002
Decision Date 12/24/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No