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FDA 510(k)

EMPOWR Revision Symmetric Knee Cones

K-Number: K240324 · 2024-04-26

ApplicantEncore Medical, L.P. (Dba Enovis)
Decision Date2024-04-26
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EMPOWR Revision Symmetric Knee Cones is a medical device manufactured by Encore Medical, L.P. (Dba Enovis). It received FDA 510(k) clearance on 2024-04-26 under approval number K240324. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMPOWR Revision Symmetric Knee Cones?

EMPOWR Revision Symmetric Knee Cones is a medical device that received FDA 510(k) clearance on 2024-04-26. It is manufactured by Encore Medical, L.P. (Dba Enovis). The 510(k) number is K240324.

When was EMPOWR Revision Symmetric Knee Cones approved by the FDA?

EMPOWR Revision Symmetric Knee Cones received FDA 510(k) clearance on 2024-04-26, under approval number K240324.

What company makes EMPOWR Revision Symmetric Knee Cones?

EMPOWR Revision Symmetric Knee Cones is manufactured by Encore Medical, L.P. (Dba Enovis).

What is the FDA product code for EMPOWR Revision Symmetric Knee Cones?

The FDA product code for EMPOWR Revision Symmetric Knee Cones is JWH.

Related Devices (Code: JWH)

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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.

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