BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES Adverse Event — Malfunction (MDR 1219602-2008-00024)
BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES Adverse Event — Malfunction (MDR 1219602-2008-00024) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES; Generic name: BIORAPTOR; Manufacturer: SMITH & NEPHEW INC., ENDOSCOPY DIV..
| Device | BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES |
|---|---|
| Generic name | BIORAPTOR |
| Manufacturer | SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| Report number | 1219602-2008-00024 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Foreign, Company representation, COMPANY REPRESENTATIVE, |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →