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Spiway, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213153SPIWay Endonasal Access GuideOctober 27, 2021
K180141SPIWay Endonasal Access GuideFebruary 16, 2018
K153686SPIWay Endonasal Access GuideJanuary 28, 2016
K132721SPIWAY ENDONASAL ACCESS GUIDEJanuary 29, 2014