Device Classification Name |
fastener, fixation, biodegradable, soft tissue
|
510(k) Number |
K173240 |
Device Name |
Arthrex PushLock |
Applicant |
Arthrex Inc. |
1370 Creekside Boulevard |
Naples,
FL
34108 -1945
|
|
Applicant Contact |
David L. Rogers |
Correspondent |
Arthrex Inc. |
1370 Creekside Boulevard |
Naples,
FL
34108 -1945
|
|
Correspondent Contact |
David L. Rogers |
Regulation Number | 888.3030
|
Classification Product Code |
|
Date Received | 10/05/2017 |
Decision Date | 01/16/2018 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|