Class Class II
MedCAD AccuPlan System (K223024)
Description
MedCAD AccuPlan System by Medcad, an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223024
Clearance Date2023-03-07
Clearance TypeTraditional
Product CodeDZJ
Regulation Number872.4120
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223024
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. MedCAD AccuPlan System (K223024) cites 3 predicate devices and is itself cited by 2 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K220357 | MedCAD AccuShape Titanium Patient-Specific Cranial Implant | Medcad | 2022 |
| K192282 | MedCAD® AccuPlan® System | Medcad | 2020 |
| K181241 | KLS Martin Individual Patient Solutions (IPS) Planning System | KLS-Martin L.P. | 2018 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241811 | MedCAD® AccuStride System | Medcad | 2025 |
| K223421 | MedCAD AccuPlan Orthopedics System | Medcad | 2023 |
Trace the full predicate network for K223024
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.