Brand Name | CARTIVA |
Type of Device | PROSTHESIS, TOE, HEMI, PHALANGEAL |
Manufacturer (Section D) |
CARTIVA, INC. |
alpharetta GA |
|
MDR Report Key | 8650689 |
MDR Text Key | 146621256 |
Report Number | MW5086959 |
Device Sequence Number | 1 |
Product Code |
KWD
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
05/23/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 05/28/2019 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was Device Evaluated by Manufacturer? |
No Information
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Disability;
|
Patient Age | 59 YR |
Patient Weight | 50 |
|
|