Class Class II
Latitud™ Hip Replacement System (K222436)
Description
Latitud™ Hip Replacement System by Meril Healthcare Pvt. , Ltd., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222436
Clearance Date2023-05-09
Clearance TypeTraditional
Product CodeLPH
Regulation Number888.3358
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222436
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. Latitud™ Hip Replacement System (K222436) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K172857 | Latitud Hip Replacement System | Meril Healthcare Pvt. , Ltd. | 2018 |
Trace the full predicate network for K222436
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.