Device Classification Name |
plate, bone
|
510(k) Number |
K122313 |
Device Name |
STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM |
Applicant |
Stryker |
750 TRADE CENTRE WAY |
STE 200 |
PORTAGE,
MI
49002
|
|
Applicant Contact |
ROB YAMASHITA |
Correspondent |
Stryker |
750 TRADE CENTRE WAY |
STE 200 |
PORTAGE,
MI
49002
|
|
Correspondent Contact |
ROB YAMASHITA |
Regulation Number | 872.4760
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 08/01/2012 |
Decision Date | 10/31/2012 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Dental
|
510k Review Panel |
Dental
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|