Device Classification Name |
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
More FDA Info for this Device |
510(K) Number |
K190633 |
Device Name |
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer |
Applicant |
NanoOrtho, LLC
860 Oak Park Blvd STE 301
Arroyo Grande, CA 93420 US
Other 510(k) Applications for this Company
|
Contact |
Austin Ferro
Other 510(k) Applications for this Contact |
Regulation Number |
888.3530
More FDA Info for this Regulation Number |
Classification Product Code |
HRY
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
03/12/2019 |
Decision Date |
12/20/2019 |
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 |
|