Device Classification Name |
interventional fluoroscopic x-ray system
|
510(k) Number |
K173664 |
Device Name |
Medtronic O-arm O2 Imaging System |
Applicant |
Medtronic Inc. |
300 Foster St |
Littleton,
MA
01460
|
|
Applicant Contact |
Dean Honkonen |
Correspondent |
Medtronic Inc. |
300 Foster St |
Littleton,
MA
01460
|
|
Correspondent Contact |
Dean Honkonen |
Regulation Number | 892.1650
|
Classification Product Code |
|
Subsequent Product Codes |
|
Date Received | 11/29/2017 |
Decision Date | 12/29/2017 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|