Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System

FDA 510(k) K242831 · Howmedica Osteonics Corp., Dba Stryker Orthopaedics

Substantially Equivalent

510(k) numberK242831

Submission

Device name
Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System
Applicant
Howmedica Osteonics Corp., Dba Stryker Orthopaedics
Mahwah, NJ, US
Received
September 19, 2024
Decision date
December 4, 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
JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3560
Specialty
Orthopedic
Implant
Yes

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K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and…JWH · Traditional B-One Ortho, Corp.09/08/2026SE
K262130ATTUNE Revision Knee SystemJWH · Traditional Depuy Orthopaedics, Inc.09/04/2026SE
K253961SK Knee SystemJWH · Traditional Just Medical Devices (Tianjin) Co., Ltd.09/01/2026SE
K261563Freedom Total Knee System (E-Poly Tibial Liners)JWH · Traditional Maxx Orthopedics, Inc.08/07/2026SE
K262251ACTIFY™ Total Knee System, ACTIFY™ 3D Total Knee System (ACTIFY MC Tibial Insert)JWH · Special Globus Medical, Inc.07/31/2026SE
K261734Klassic Infection Spacer SystemJWH · Traditional Total Joint Orthopedics, Inc.07/23/2026SE
K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemJWH · Traditional DePuy Ireland UC06/25/2026SE
K261032NovoKnee (SteriKnee)JWH · Special NovoSource04/27/2026SE

More from NovoSource

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K261898Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee SystemKRO · Traditional 08/06/2026SE
K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained…LPH · Traditional 07/10/2026SE
K253637Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing InsertMBH · Traditional 02/18/2026SE
K252898Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella…KRO · Traditional 12/15/2025SE
K252044Triathlon® Total Knee System - Triathlon® Gold Femoral ComponentsMBH · Traditional 10/24/2025SE
K251665Triathlon® Hinge Knee SystemKRO · Traditional 07/25/2025SE
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K243817Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior…JWH · Traditional 02/06/2025SE
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Questions and answers

When was Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System cleared by the FDA?

Triathlon Knee System; Triathlon Pro Posterior Stabilized Femoral Components; Triathlon Tritanium Tibial Baseplate; Triathlon Low Profile Tibial Tray; Triathlon Metal Backed Patella; Triathlon Partial Knee System; Avon Patello-femoral Joint Prosthesis; Restoris Multi-Compartmental Knee System (K242831) received a 510(k) decision of Substantially Equivalent on December 4, 2024, 76 days after the submission was received.

What is the product code of K242831?

The FDA product code is JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3560.