Stryker Orthopaedics Hip Devices Labeling Update (K243784)
Description
Stryker Orthopaedics Hip Devices Labeling Update by Howmedica Osteonics Corp., Dba Stryker Orthopaedics, an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243784
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. Stryker Orthopaedics Hip Devices Labeling Update (K243784) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233498 | Stryker Orthopaedics Hip Systems Labeling Update | Howmedica Osteonics Corp., Dba Stry... | 2023 |
| K121308 | HIP SYSTEMS | Howmedica Osteonics Corp. | 2012 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K250989 | Stryker and Serf hip devices | Howmedica Osteonics Corp (Dba Stryk... | 2025 |
Trace the full predicate network for K243784
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.