Device Classification Name |
intervertebral fusion device with bone graft, lumbar
|
510(k) Number |
K131350 |
Device Name |
CALIX LUMBAR SPINAL IMPLANT SYSTEM |
Applicant |
X-SPINE SYSTEMS, INC |
452 Alexandersville Rd |
Miamisburg,
OH
45342
|
|
Applicant Contact |
DAVID KIRSCHMAN |
Correspondent |
X-SPINE SYSTEMS, INC |
452 Alexandersville Rd |
Miamisburg,
OH
45342
|
|
Correspondent Contact |
DAVID KIRSCHMAN |
Regulation Number | 888.3080
|
Classification Product Code |
|
Date Received | 05/10/2013 |
Decision Date | 10/23/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|