| Device Classification Name |
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
More FDA Info for this Device |
| 510(K) Number |
K062861 |
| Device Name |
Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented |
| Applicant |
ASCENSION ORTHOPEDICS, INC.
8700 CAMERON RD., STE. 100
AUSTIN, TX 78754-3832 US
Other 510(k) Applications for this Company
|
| Contact |
GLEN NEALLY
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 |
09/25/2006 |
| Decision Date |
10/31/2006 |
| 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 |
|