Device Classification Name |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K140749 |
Device Name |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer |
Applicant |
WRIGHT MEDICAL TECHNOLOGY, INC.
1023 CHERRY ROAD
MEMPHIS, TN 38117 US
Other 510(k) Applications for this Company
|
Contact |
JEANINE REDDEN
Other 510(k) Applications for this Contact |
Regulation Number |
888.3110
More FDA Info for this Regulation Number |
Classification Product Code |
HSN
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
03/25/2014 |
Decision Date |
04/25/2014 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Summary |
Type |
Special |
Reviewed By Third Party |
N |
Expedited Review |
|