FDA 510(k) Applications Submitted by Keith Neligan
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170636 | 03/02/2017 | Fathom-16 Steerable Guidewires | Boston Scientific Corporation |
| K211508 | 05/14/2021 | Steinmann Pins and Kirschner Wires | Stryker GmbH |
| K212581 | 08/16/2021 | VariAx 2 Distal Radius System, VariAx 2 Distal Ulna System | Stryker GmbH |
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