Brand Name | LEGACY 3 IMPLANT |
Type of Device | DENTAL IMPLANT |
Manufacturer (Section D) |
IMPLANT DIRECT SYBRON MANUFACTURING LLC |
3050 east hillcrest drive |
thousand oaks CA 91262 |
|
Manufacturer Contact |
kai
diaz
|
3050 east hillcrest drive |
thousand oaks, CA 91262
|
8184443300
|
|
MDR Report Key | 8952119 |
MDR Text Key | 156257972 |
Report Number | 3001617766-2019-01060 |
Device Sequence Number | 1 |
Product Code |
DZE
|
UDI-Device Identifier | 10841307101994 |
UDI-Public | 10841307101994 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K090234 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional,user faci |
Reporter Occupation |
Dentist
|
Type of Report
| Initial |
Report Date |
08/30/2019 |
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
|
Device Expiration Date | 11/15/2016 |
Device Catalogue Number | 853210 |
Device Lot Number | 33821 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
07/31/2019
|
Initial Date FDA Received | 08/30/2019 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 11/16/2011 |
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;
|
Patient Age | 59 YR |
|
|