Meduloc Intramedullary Fracture Fixation (IFF) System

FDA 510(k) K250316 · Meduloc, LLC

Substantially Equivalent

510(k) numberK250316

Submission

Device name
Meduloc Intramedullary Fracture Fixation (IFF) System
Applicant
Meduloc, LLC
Del Mar, CA, US
Received
February 4, 2025
Decision date
October 29, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JDW – Pin, Fixation, Threaded
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3040
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code JDW

510(k)DeviceApplicantDecision
K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmJDW · Special Biodynamik, Inc.02/10/2026SE
K241357XT3 SystemJDW · Traditional Biodynamik, Inc.01/22/2025SE
K223112MAVERICK Mini External Fixation SystemJDW · Traditional Smith & Nephew, Inc.12/08/2022SE
K213874MAVERICK External Fixation SystemJDW · Traditional Smith & Nephew, Inc.02/11/2022SE
K211508Steinmann Pins and Kirschner WiresJDW · Traditional Stryker GmbH10/05/2021SE
K210784Extended HA Half PinsJDW · Special Smith & Nephew, Inc.04/02/2021SE
K200933Syntec Non-Sterile Steinmann Pins SystemJDW · Special Syntec Scientific Corporation05/05/2020SE
K191803Orthopedic Fixation PinJDW · Traditional Tinavi (Anhui) Medical Technologies Co., Ltd.04/14/2020SE
K192768Temporary Fixation PinsJDW · Traditional Eisertech, LLC12/26/2019SE
K182171SMV Scientific K-Wire and PinsJDW · Traditional Summit Medventures10/25/2018SE

Questions and answers

When was Meduloc Intramedullary Fracture Fixation (IFF) System cleared by the FDA?

Meduloc Intramedullary Fracture Fixation (IFF) System (K250316) received a 510(k) decision of Substantially Equivalent on October 29, 2025, 267 days after the submission was received.

What is the product code of K250316?

The FDA product code is JDW – Pin, Fixation, Threaded, a Class II (moderate risk) device regulated under 21 CFR 888.3040.