Intramedullary Bone Plug

FDA 510(k) K832328 · Kirschner Medical Corp.

Substantially Equivalent

510(k) numberK832328

Submission

Device name
Intramedullary Bone Plug
Applicant
Kirschner Medical Corp.
Mchenry, IL, US
Received
July 15, 1983
Decision date
October 20, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JDS – Nail, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code JDS

510(k)DeviceApplicantDecision
K243608TRIGEN Stable Lock Nut & WasherJDS · Traditional Smith & Nephew, Inc.06/12/2025SE
K240061TRIGEN MAX Tibial Nail System; INTERTAN MAX Hip Fracture Nail SystemJDS · Traditional Smith & Nephew, Inc.09/20/2024SE
K241804TRIGEN INTERTAN 10S Nail SystemJDS · Traditional Smith & Nephew, Inc.08/22/2024SE
K233150NET BRAND Osteosynthesis Nailing SystemJDS · Traditional Narang Medical , Ltd.02/20/2024SE
K230761TRIGEN META-NAIL Nail SystemJDS · Traditional Smith & Nephew, Inc.06/14/2023SE
K201336DePuy Synthes Tibial Nail Advanced, Depuy Synthes Locking Screws Medullary Nails, 4.0…JDS · Traditional Synthes (USA) Products, LLC09/03/2020SE
K192003Auxein Nailing SystemJDS · Traditional Auxein Medical Private Limited06/10/2020SE
K193533WIN Flexible Nail SystemJDS · Traditional Biomet, Inc.02/20/2020SE
K141737Conventus PHS SystemJDS · Traditional Conventus Orthopaedics, Inc.04/08/2015SE
K123948China Nails and AccessoriesJDS · Traditional Smith & Nephew, Inc.03/14/2013SE

More from Smith & Nephew, Inc.

510(k)DeviceDecision
K940537Kirschner(R) Modular Ii-C(Tm) Total Shoulder SystemKWT · Traditional 08/29/1995SE
K936274Kirschner Performance Posterior Stabilized Total Knee SystemJWH · Traditional 01/18/1995SE
K942891Summit Total Hip SystemMEH · Traditional 11/02/1994SE
K941486Integrity Total Hip System, Non-PorousJDI · Traditional 09/20/1994SE
K933843Line Extension for Kirschner Performance Total Knee System, Porous CoatedJWH · Traditional 08/05/1994SE
K935951Kirschner C-2 Osteocap Total Hip SystemJDI · Traditional 07/18/1994SE
K935206Kirschner Integrity Acetabular Cup ModificationJDI · Traditional 07/13/1994SE
K934589Kirschner Performance Total Knee System Porous CoatedJWH · Traditional 07/13/1994SN
K934694Kirschner Zirconia Femoral HeadLZO · Traditional 05/18/1994SE
K920188Threaded PinsMBJ · Traditional 05/12/1993SE

Questions and answers

When was Intramedullary Bone Plug cleared by the FDA?

Intramedullary Bone Plug (K832328) received a 510(k) decision of Substantially Equivalent on October 20, 1983, 97 days after the submission was received.

What is the product code of K832328?

The FDA product code is JDS – Nail, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.