Device Classification Name |
prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
|
510(k) Number |
K171365 |
Device Name |
Arthrex Knee Systems |
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 | 888.3565
|
Classification Product Code |
|
Subsequent Product Codes |
|
Date Received | 05/09/2017 |
Decision Date | 11/07/2017 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|