EMPOWR Acetabular® Liner Extension
K-Number: K251833 · 2025-11-12
ApplicantEncore Medical L.P.
Decision Date2025-11-12
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
EMPOWR Acetabular® Liner Extension is a medical device manufactured by Encore Medical L.P.. It received FDA 510(k) clearance on 2025-11-12 under approval number K251833. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EMPOWR Acetabular® Liner Extension?
EMPOWR Acetabular® Liner Extension is a medical device that received FDA 510(k) clearance on 2025-11-12. It is manufactured by Encore Medical L.P.. The 510(k) number is K251833.
When was EMPOWR Acetabular® Liner Extension approved by the FDA?
EMPOWR Acetabular® Liner Extension received FDA 510(k) clearance on 2025-11-12, under approval number K251833.
What company makes EMPOWR Acetabular® Liner Extension?
EMPOWR Acetabular® Liner Extension is manufactured by Encore Medical L.P..
What is the FDA product code for EMPOWR Acetabular® Liner Extension?
The FDA product code for EMPOWR Acetabular® Liner Extension is LPH.
Other Devices by Encore Medical L.P.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.