Class Class II
Equinoxe® Shoulder System (K243448)
Description
Equinoxe® Shoulder System by Exactech, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243448
Clearance Date2025-08-01
Clearance TypeTraditional
Product CodePHX
Regulation Number888.3660
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243448
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. Equinoxe® Shoulder System (K243448) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223833 | Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adap... | Exactech, Inc. | 2023 |
| K232002 | Vantage® Total Ankle System | Exactech, Inc. | 2023 |
Trace the full predicate network for K243448
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.