Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Spiway, LLC

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest FDA decision2021-10-27
TypeNumberDevice NameCodeDateActions
510(k) K213153 SPIWay Endonasal Access GuideLYA2021-10-27 View
510(k) K180141 SPIWay Endonasal Access GuideLYA2018-02-16 View
510(k) K153686 SPIWay Endonasal Access GuideLYA2016-01-28 View
↑