Device recall
Z-0396-2007: Perry-Kolberg Titanium Motility/Support System (Threaded Sleeve and Flat Peg)…
FDA device recall · Class II · Integrated Orbital Implants Inc
Key facts
| Recall number (Z-number) | Z-0396-2007 |
|---|---|
| Recall event | 37139 |
| Product | Perry-Kolberg Titanium Motility/Support System (Threaded Sleeve and Flat Peg), Model Number 100045 The threaded sleeve and flat peg are two components of the P-K Titanium Motility/Support System. The threaded sleeve is an externally threaded cylinder and an internal drilled hole designed to receive… |
| Product code | MQU |
| Recalling firm | Integrated Orbital Implants Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 12, 2007 |
| 510(k) numbers | K974203 |
| FEI number | 3009688114 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database