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Novastep

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
1
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K230724arcad® 2.0 Duo & Quadro osteosynthesis compressive staplesDecember 4, 2023
K223468Nexis® compressive screwsAugust 30, 2023
K192356Airlock Centrolock Osteosynthesis Implant SystemDecember 14, 2019
K151277Airlock® osteosynthesis plate systemAugust 13, 2015
K143523Airlock osteosynthesis plate systemApril 6, 2015
K143049LYNC intramedullary implantFebruary 19, 2015
K143229Nexis osteosynthesis compressive screwsFebruary 6, 2015
K143146Nexis osteosynthesis snap-off screwsFebruary 6, 2015