Brand Name | CARTIVA IMPLANT |
Type of Device | PROSTHESIS, METATARSOPHALANGEAL JOINT CARTILAGE REPLACEMENT IMPLANT |
Manufacturer (Section D) |
CARTIVA, INC |
6120 windward parkway |
suite 220 |
alpharetta GA 30005 |
|
Manufacturer (Section G) |
CARTIVA, INC |
6120 windward parkway |
suite 220 |
alpharetta GA 30005 |
|
Manufacturer Contact |
matthew
parrish
|
1023 cherry rd |
memphis, TN 38117
|
|
MDR Report Key | 11178377 |
MDR Text Key | 227068257 |
Report Number | 3009351194-2021-00071 |
Device Sequence Number | 1 |
Product Code |
PNW
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | P150017 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
consumer |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
12/18/2020 |
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? |
Yes
|
Device Operator |
Health Professional
|
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
12/18/2020
|
Initial Date FDA Received | 01/15/2021 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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) |
Other;
Required Intervention;
|