| Brand Name | ACROMIONIZER,4.0 EP-1,DSPL BL |
| Common Device Name | SAW, POWERED, AND ACCESSORIES |
| Manufacturer (Section D) |
| SMITH & NEPHEW, INC. |
| 130 forbes boulevard |
| mansfield MA 02048 |
|
| MDR Report Key | 7814697 |
| Report Number | 1219602-2018-01117 |
| Device Sequence Number | 1290919 |
| Product Code |
HAB
|
| UDI-Device Identifier | 03596010251541 |
| UDI-Public | (01)03596010251541(17)220707(10)50673387 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | CH |
| PMA/510(K) Number | EXEMPT |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
company representative,distri |
| Initial Reporter Occupation |
Non-Healthcare Professional
|
| Type of Report
| Initial,Followup |
| Report Date (Section B) |
09/21/2018 |
| 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
|
| Operator of Device |
Health Professional
|
| Device Expiration Date | 07/07/2022 |
| Device Model Number | 7205326 |
| Device Catalogue Number | 7205326 |
| Device Lot Number | 50673387 |
| Was Device Available for Evaluation? |
No
|
| Initial Date Received by Manufacturer | 07/30/2018 |
| Supplement Date Received by Manufacturer | 09/19/2018
|
| Initial Report FDA Received Date | 08/24/2018 |
| Supplement Report FDA Received Date | 09/21/2018
|
| Patient Sequence Number | 1 |
|
|