Device Classification Name |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K222835 |
Device Name |
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer |
Applicant |
Wright Medical Technology, Inc.
10801 Nesbitt Ave S.
Bloomington, MN 55437 US
Other 510(k) Applications for this Company
|
Contact |
Paxia Her
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 |
09/20/2022 |
Decision Date |
01/27/2023 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
OR - Orthopedic |
Review Advisory Committee |
OR - Orthopedic |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|