Device Classification Name |
Prosthesis, Elbow, Hemi-, Radial, Polymer
More FDA Info for this Device |
510(K) Number |
K030237 |
Device Name |
Prosthesis, Elbow, Hemi-, Radial, Polymer |
Applicant |
KAPP SURGICAL INSTRUMENT, INC.
4919 WARRENSVILLE CENTER RD.
CLEVELAND, OH 44128 US
Other 510(k) Applications for this Company
|
Contact |
ALBERT SANTILLI
Other 510(k) Applications for this Contact |
Regulation Number |
888.3170
More FDA Info for this Regulation Number |
Classification Product Code |
KWI
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
01/23/2003 |
Decision Date |
08/29/2003 |
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 |
|