Device Classification Name |
Posterior Metal/Polymer Spinal System, Fusion
|
510(k) Number |
K071879 |
Device Name |
ZIMMER DTO IMPLANT |
Applicant |
ZIMMER SPINE, INC |
7375 BUSH LAKE RD. |
MINNEAPOLIS,
MN
55441
|
|
Applicant Contact |
NICOLE BOWDEN |
Correspondent |
ZIMMER SPINE, INC |
7375 Blush Lake Rd |
Minneapolis,
MN
55441
|
|
Correspondent Contact |
Nicole Bowden |
Regulation Number | 888.3070
|
Classification Product Code |
|
Date Received | 07/09/2007 |
Decision Date | 10/05/2007 |
Decision |
SE - With Limitations
(SESU) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|