EMPHASYS Acetabular Shell with RapiTite HA

FDA 510(k) K242084 · Depuy Ireland UC

Substantially Equivalent

510(k) numberK242084

Submission

Device name
EMPHASYS Acetabular Shell with RapiTite HA
Applicant
Depuy Ireland UC
Cork, IE
Received
July 16, 2024
Decision date
October 7, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3358
Specialty
Orthopedic
Implant
Yes

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K252623G7® Revision Acetabular SystemLPH · Traditional Zimmer, Inc.02/04/2026SE
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More from Encore Medical L.P.

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K253624INHANCE™ Reverse Shoulder SystemPHX · Traditional 03/11/2026SE
K253551VELYS™ Hip NavigationQIH · Traditional 03/06/2026SE
K253197ATTUNE™ Total Knee System; ATTUNE™ Revision Sleeve LPS™ Femoral AdaptorsJWH · Traditional 11/19/2025SE
K251292RECLAIM Monobloc Revision Femoral StemLZO · Special 05/23/2025SE
K243977EMPHASYS Acetabular SystemLPH · Special 01/22/2025SE
K243248Inhance Intact™PKC · Traditional 12/23/2024SE
K242871ATTUNE™ Revision Hinge KneeKRO · Traditional 11/21/2024SE

Questions and answers

When was EMPHASYS Acetabular Shell with RapiTite HA cleared by the FDA?

EMPHASYS Acetabular Shell with RapiTite HA (K242084) received a 510(k) decision of Substantially Equivalent on October 7, 2024, 83 days after the submission was received.

What is the product code of K242084?

The FDA product code is LPH – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3358.