Device recall
Z-3033-2011: PERPOS PLS, CATALOG #'s 9045-01 & 9045-02 A sterile, medical device kit…
FDA device recall · Class II · Interventional Spine Inc
Key facts
| Recall number (Z-number) | Z-3033-2011 |
|---|---|
| Recall event | 58381 |
| Product | PERPOS PLS, CATALOG #'s 9045-01 & 9045-02 A sterile, medical device kit consisting of the components listed in Table 1-1 below. The kit is used by medical professionals to stabilize the spine as an aid to fusion through immobilization of the facet joints. |
| Product code | MRW |
| Recalling firm | Interventional Spine Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 11, 2013 |
| 510(k) numbers | K062391 |
| FEI number | 3003523239 |
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