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Fixation Accessory
FDA product code LYT · Class 2 · Orthopedic
49
Registered devices
31
Adverse events
4
Recalls
9
510(k) clearances
Devices with this code
Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Halo Systems — OSSUR AMERICAS, INC.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Halo Systems — OSSUR AMERICAS, INC.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Dall-Miles — Howmedica Osteonics Corp.Halo Systems — OSSUR AMERICAS, INC.Dall-Miles — Howmedica Osteonics Corp.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-06-21 | Ossur Americas | Halo system products labeled MR conditional will undergo confirmatory safety testing to confirm MR conditional parameters. In addition, the second line descript |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
| 2008-09-26 | Ossur | Ossur has initiated this voluntary recall as a precautionary measure because the firm is unable to guarantee the sterility of the affected products. |
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