Device Classification Name |
Plate, Fixation, Bone
|
510(k) Number |
K973812 |
Device Name |
ARTHREX PUDDU OSTEOTOMY SYSTEM |
Applicant |
ARTHREX, INC. |
2885 SOUTH HORSESHOE DR. |
NAPLES,
FL
34104
|
|
Applicant Contact |
SCOTT M DURLACHER |
Correspondent |
ARTHREX, INC. |
2885 SOUTH HORSESHOE DR. |
NAPLES,
FL
34104
|
|
Correspondent Contact |
SCOTT M DURLACHER |
Regulation Number | 888.3030
|
Classification Product Code |
|
Date Received | 10/07/1997 |
Decision Date | 06/10/1998 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|