iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating

FDA 510(k) K243192 · Nextstep Arthopedix, LLC

Substantially Equivalent

510(k) numberK243192

Submission

Device name
iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating
Applicant
Nextstep Arthopedix, LLC
Akron, OH, US
Received
September 30, 2024
Decision date
June 5, 2026
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

Other 510(k)s with product code LPH

510(k)DeviceApplicantDecision
K253630Mpact 3D Metal FoamLPH · Traditional Medacta International S.A.08/28/2026SE
K254043TRIVANCE™ Hip StemLPH · Traditional Globus Medical, Inc.08/04/2026SE
K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained…LPH · Traditional Howmedica Osteonics Corp., Dba Stryker…07/10/2026SE
K251270Taperloc® Complete Hip StemLPH · Traditional Biomet, Inc.05/19/2026SE
K252623G7® Revision Acetabular SystemLPH · Traditional Zimmer, Inc.02/04/2026SE
K251043Mpact 3D Metal Implants Extension – DMLS TechnologyLPH · Traditional Medacta International S.A.01/28/2026SE
K252067Velora Acetabular SystemLPH · Traditional Restor3D, Inc.12/05/2025SE
K252846TaperSet™ Hip SystemLPH · Special Shalby Advanced Technologies, Inc. Dba Consensus…11/20/2025SE
K251833EMPOWR Acetabular® Liner ExtensionLPH · Traditional Encore Medical L.P.11/12/2025SE
K251718ArTT Augments and Buttresses and Bone ScrewsLPH · Traditional Lima Corporate S.P.A.08/29/2025SE

Questions and answers

When was iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating cleared by the FDA?

iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating (K243192) received a 510(k) decision of Substantially Equivalent on June 5, 2026, 613 days after the submission was received.

What is the product code of K243192?

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.