Home › Device types › HAX
Tong, Skull For Traction
FDA product code HAX · Class 2 · Neurology
2,246
Registered devices
26
Adverse events
13
Recalls
20
510(k) clearances
Devices with this code
PMT® Halo Systems — PMT CORPORATIONHALO VEST LINER — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONSymmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.PMT® CORPORATION HALO — PMT CORPORATIONPMT® CORPORATION HALO — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® CORPORATION HALO — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® CORPORATION HALO — PMT CORPORATIONPMT® CORPORATION HALO — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATIONPMT® CORPORATION HALO — PMT CORPORATIONPMT® Halo Systems — PMT CORPORATION
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 |
| 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 |
| 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 |
| 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 |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
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