Class Class II

AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System (K251184)

K251184 2025-05-16 Special
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Description

AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System by Encore Medical, L.P., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251184
Clearance Date2025-05-16
Clearance TypeSpecial
Product CodePHX
Regulation Number888.3660

Categories

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Predicate lineage for K251184

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. AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System (K251184) cites 5 predicate devices and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K233481AltiVate ReverseĀ® GlenoidEncore Medical L.P.2024
K142139SMR 40MM GLENOSPHERELima Corporate S.P.A.2014
K141006RSP HUMERAL SOCKET INSERTDjo Global2014
K110598SMR REVERSE SHOULDER SYSTEMLima Corporate S.P.A.2011
K051075ENCORE REVERSE SHOULDER PROSTHESISEncore Medical L.P.2005

Trace the full predicate network for K251184

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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