TaperSet™ Hip System

FDA 510(k) K252846 · Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics

Substantially Equivalent

510(k) numberK252846

Submission

Device name
TaperSet™ Hip System
Applicant
Shalby Advanced Technologies, Inc. Dba Consensus Orthopedics
El Dorado Hills, CA, US
Received
September 8, 2025
Decision date
November 20, 2025
Decision
Substantially Equivalent (SESE)
Type
Special 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
K251043Mpact 3D Metal Implants Extension – DMLS TechnologyLPH · Traditional Medacta International S.A.01/28/2026SE
K252067Velora Acetabular SystemLPH · Traditional Restor3D, Inc.12/05/2025SE
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Questions and answers

When was TaperSet™ Hip System cleared by the FDA?

TaperSet™ Hip System (K252846) received a 510(k) decision of Substantially Equivalent on November 20, 2025, 73 days after the submission was received.

What is the product code of K252846?

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.