Brand Name | QUINTEX SEMICONSTRAINED SCREW 4.0X16MM |
Type of Device | BONE SCREW |
Manufacturer (Section D) |
AESCULAP IMPLANT SYSTEMS |
po box 40 |
tuttlingen, 78501 |
GM 78501 |
|
Manufacturer (Section G) |
AESCULAP IMPLANT SYSTEMS |
po box 40 |
|
tuttlingen, 78501 |
GM
78501
|
|
Manufacturer Contact |
nicole
broyles
|
615 lambert pointe drive |
hazelwood, MO 63042
|
3145515988
|
|
MDR Report Key | 5112495 |
MDR Text Key | 27150463 |
Report Number | 3005673311-2015-00146 |
Device Sequence Number | 1 |
Product Code |
KWQ
|
Combination Product (y/n) | N |
Reporter Country Code | GM |
PMA/PMN Number | K100243 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Other
|
Type of Report
| Followup |
Report Date |
03/16/2016 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
No Information
|
Device Model Number | SC503T |
Device Catalogue Number | SC503T |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 09/29/2015 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 03/22/2016
|
Was Device Evaluated by Manufacturer? |
Yes
|
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;
|
|
|