Class Class II

MySpine WebPlanner (K243697)

K243697 2025-04-23 Traditional
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Description

MySpine WebPlanner by Medacta International S.A., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243697
Clearance Date2025-04-23
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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Predicate lineage for K243697

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. MySpine WebPlanner (K243697) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K211386MySpine WebPlanner & MyBalanceMedacta International S.A.2021

Trace the full predicate network for K243697

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.

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