HIPLOC COMPRESSION HIP SCREW


Device Classification Name

device, fixation, proximal femoral, implant

510(k) Number K080685
Device Name HIPLOC COMPRESSION HIP SCREW
Applicant
BIOMET MANUFACTURING, INC.
p.o. box 587
warsaw, 
IN 
46581 -0578

Applicant Contact becky earl
Correspondent
BIOMET MANUFACTURING, INC.
p.o. box 587
warsaw, 
IN 
46581 -0578

Correspodent Contact becky earl
Regulation Number 888.3030
Classification Product Code
JDO  
Subsequent Product Code
KTT  
Date Received 03/11/2008
Decision Date 08/15/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

Orthopedic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No