Brand Name | RSP |
Type of Device | GLENOID, HEAD W/RETAINING SCREW, RSP, 36MM, NEUTRAL |
Manufacturer (Section D) |
ENCORE MEDICAL L.P. |
9800 metric blvd. |
austin, tx 78758-5445 |
|
MDR Report Key | 10516945 |
MDR Text Key | 206481457 |
Report Number | 1644408-2020-00790 |
Device Sequence Number | 1 |
Product Code |
PHX
|
UDI-Device Identifier | 00888912024761 |
UDI-Public | (01)00888912024761 |
Combination Product (y/n) | N |
PMA/PMN Number | K051075 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative |
Type of Report
| Initial,Followup |
Report Date |
10/08/2020 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 09/10/2020 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 10/16/2023 |
Device Model Number | 508-36-101 |
Device Catalogue Number | 508-36-101 |
Device Lot Number | 869C2307 |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 09/10/2020 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
|
|
|