Device recall
Z-1047-2019: Avitus Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone…
FDA device recall · Class II · Avitus Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1047-2019 |
|---|---|
| Recall event | 82271 |
| Product | Avitus Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus Bone Harvester is intended to harvest cancellous bone and bone marrow |
| Product code | KNW |
| Recalling firm | Avitus Orthopaedics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2020 |
| 510(k) numbers | K170539 |
| FEI number | 3011504993 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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