Brand Name | COBRA FUSION 150 ABLATION SYSTEM |
Type of Device | COBRA FUSION 150 ABLATION SYSTEM |
Manufacturer (Section D) |
ATRICURE, INC. |
7555 innovation way |
mason OH 45040 |
|
Manufacturer (Section G) |
ATRICURE, INC. |
7555 innovation way |
|
mason OH 45040 |
|
Manufacturer Contact |
anupam
bedi
|
7555 innovation way |
mason, OH
|
|
MDR Report Key | 7404009 |
MDR Text Key | 104599994 |
Report Number | 3011706110-2018-00144 |
Device Sequence Number | 1 |
Product Code |
OCL
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K113475 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
04/06/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Other Health Care Professional
|
Device Model Number | 001-700-001S |
Device Catalogue Number | 001-700-001S |
Device Lot Number | UNKNOWN |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
03/22/2018
|
Initial Date FDA Received | 04/06/2018 |
Was Device Evaluated by Manufacturer? |
No
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|