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Orthosoft D/B/A Zimmer Cas

FDA Regulatory Profile

Orthosoft D/B/A Zimmer Cas appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 16, 2023.

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Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232533ROSA Partial Knee SystemNov 16, 2023
K230243ROSA® Knee SystemMar 29, 2023
K221928ROSA® Knee SystemOct 4, 2022
K213033iASSIST Knee SystemJan 14, 2022
K210998ROSA Hip SystemAug 17, 2021
K210653ONE Planner HipJul 7, 2021
K210121ROSA Partial Knee SystemApr 19, 2021

FDA data resources