Patient Specific Distal Femoral
FDA 510(k) K140898 · Stanmore Implants Worldwide , Ltd.
510(k) numberK140898
Submission
- Device name
- Patient Specific Distal Femoral
- Applicant
- Stanmore Implants Worldwide , Ltd.
Plymouth, MA, US - Received
- April 8, 2014
- Decision date
- January 20, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3510
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KRO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261898 | Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee SystemKRO · Traditional | Howmedica Osteonics Corp. dba Stryker Orthopaedics | 08/06/2026SE |
| K252898 | Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella…KRO · Traditional | Howmedica Osteonics Corp., Dba Stryker… | 12/15/2025SE |
| K252303 | Stem Extension Line (USTAR II System)KRO · Special | United Orthopedic Corporation | 08/22/2025SE |
| K251665 | Triathlon® Hinge Knee SystemKRO · Traditional | Howmedica Osteonics Corp., Dba Stryker… | 07/25/2025SE |
| K242871 | ATTUNE Revision Hinge KneeKRO · Traditional | Depuy Ireland UC | 11/21/2024SE |
| K240043 | EVOLUTION® Hinge Knee System;GUARDIAN limb Salvage System;DCW Modular Distal Femoral…KRO · Traditional | Microport Orthopedics, Inc. | 04/01/2024SE |
| K233980 | ATTUNE Total Knee System, ATTUNE Cementless Knee System, LPS Limb Preservation System…KRO · Traditional | Depuy Ireland UC | 03/21/2024SE |
| K230563 | EVOLUTION® Hinge Knee SystemKRO · Traditional | Microport Orthopedics, Inc. | 09/27/2023SE |
| K230416 | Triathlon® Hinge Knee System; Triathlon® Revision Insert X3®KRO · Traditional | Stryker | 05/19/2023SE |
| K223069 | Modular Rotating Hinge Knee Systems and Compatible ComponentsKRO · Traditional | Howmedica Osteonics Corp., Dba Stryker… | 04/21/2023SE |
More from Howmedica Osteonics Corp., Dba Stryker Orthopaedics
| 510(k) | Device | Decision |
|---|---|---|
| K133152 | JTS Extendible Distal Femoral ImplantKRO · Special | 01/22/2014SE |
| K121765 | Sculptor Robotic Guidance Arm (Rga)OLO · Traditional | 01/11/2013SE |
| K121056 | Mets Modular Proximal FemurJDI · Traditional | 09/20/2012SE |
| K121055 | Mets Modular Total FemurJDI · Traditional | 09/19/2012SE |
| K121029 | Mets Modular Distal FemurKRO · Traditional | 09/19/2012SE |
| K120992 | Mets Smiles Total Knee ReplacementKRO · Traditional | 09/05/2012SE |
| K092138 | JTS Extendeable ImplantKRO · Traditional | 03/22/2011SE |
Questions and answers
When was Patient Specific Distal Femoral cleared by the FDA?
Patient Specific Distal Femoral (K140898) received a 510(k) decision of Substantially Equivalent on January 20, 2015, 287 days after the submission was received.
What is the product code of K140898?
The FDA product code is KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3510.