Brand Name | HTR-PEKK |
Type of Device | CRANIAL IMPLANT |
Manufacturer (Section D) |
OXFORD PERFORMANCE MATERIALS, INC. |
30 south satellite road |
south windsor CT 06074 |
|
Manufacturer (Section G) |
OXFORD PERFORMANCE MATERIALS, INC. |
30 south satellite road |
|
south windsor CT 06074 |
|
Manufacturer Contact |
james
porteus
|
30 south satellite road |
south windsor, CT 06074
|
8606569438
|
|
MDR Report Key | 16499649 |
MDR Text Key | 310853762 |
Report Number | 3009582362-2023-00003 |
Device Sequence Number | 1 |
Product Code |
GXN
|
UDI-Device Identifier | 00810077248515 |
UDI-Public | (01)00810077248515(10)211978 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K180064 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Distributor |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
02/16/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/07/2023 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | PK625635 |
Device Lot Number | 211978 |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 02/08/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 11/18/2022 |
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;
|