Cleared Abbreviated

K073175 - JOURNEY UNICONDYLAR FEMORAL IMPLANT

K073175 is the FDA 510(k) clearance for JOURNEY UNICONDYLAR FEMORAL IMPLANT by Smith & Nephew, Inc.. It is a Class 2 Orthopedic device (product code HSX) cleared through the Abbreviated 510(k) pathway after a 37-day FDA review.

K073175 · Smith & Nephew, Inc. · Orthopedic device
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Dec 2007
Decision
37d
Days
Class 2
Risk

K073175 is an FDA 510(k) clearance for the JOURNEY UNICONDYLAR FEMORAL IMPLANT. Classified as Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer (product code HSX), Class II - Special Controls.

Submitted by Smith & Nephew, Inc. (Memphis, US). The FDA issued a Cleared decision on December 20, 2007 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3520 - the FDA orthopedic device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Smith & Nephew, Inc. devices

Submission Details

510(k) Number K073175 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 13, 2007
Decision Date December 20, 2007
Days to Decision 37 days
Submission Type Abbreviated
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 122d · This submission: 37d
Pathway characteristics
Standards-based clearance path.

Device Classification

Product Code HSX Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3520
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HSX Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer

All 99
Devices cleared under the same product code (HSX) and FDA review panel - the closest regulatory comparables to K073175.
MAKO SURGICAL CORPORATION UNICONDYLAR KNEE IMPLANT SYSTEM III
K082081 · Mako Surgical Corp. · Oct 2008
MODIFICATION TO JOURNEY UNICONDYLAR FEMORAL IMPLANT
K081351 · Smith & Nephew, Inc. · Jul 2008
MAKO SURGICAL CORP. UNICONDYLAR KNEE IMPLANT SYSTEM II
K080368 · Mako Surgical Corp. · Jun 2008
MODIFICATION TO:MAKO SURGICAL UNICONDYLAR KNEE SYSTEM
K073248 · Mako Surgical Corp. · Dec 2007
CONFORMIS UNI-CONDYLAR KNEE SYSTEM
K072586 · Conformis, Inc. · Nov 2007
CONFORMIS METAL BACKED TIBIAL COMPONENT
K072368 · Conformis, Inc. · Sep 2007