FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EMPOWR Acetabular® Liner Extension

K Number: K251833 · Decision Nov 12, 2025
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
81
Review Days
149

Basic Information

Device Name
EMPOWR Acetabular® Liner Extension
K Number
K251833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Encore Medical L.P.
Date Received
June 16, 2025
Decision Date
November 12, 2025
Product Code
LPH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LPH), ordered by most recent decision date.

View all

Other Clearances by Encore Medical L.P.

K Number Device Name
K252567 AltiVate Reverse® ADLC Glenosphere
K252974 EMPOWR Knee
K252141 AltiVate Reverse® Glenoid
K251776 EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)
K251241 EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)
K251184 AltiVate Reverse Shoulder System; RSP Shoulder System; SMR Shoulder System; PRIMA Humeral System; PRIMA Glenoid System
K241483 ceramys™ femoral head system
K233481 AltiVate Reverse® Glenoid
K222592 AltiVate® Anatomic Shoulder AG e+™ with Markers
K213387 AltiVate® Anatomic Shoulder AG e+™ with Markers
Search all 81 clearances from Encore Medical L.P. →