Device Classification Name |
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
More FDA Info for this Device |
510(K) Number |
K130675 |
Device Name |
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented |
Applicant |
ARTHREX, INC.
1370 CREEKSIDE BLVD.
NAPLES, FL 34108-1945 US
Other 510(k) Applications for this Company
|
Contact |
COURTNEY SMITH
Other 510(k) Applications for this Contact |
Regulation Number |
888.3690
More FDA Info for this Regulation Number |
Classification Product Code |
HSD
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
03/13/2013 |
Decision Date |
10/30/2013 |
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 |
|