NET BRAND Osteosynthesis Nailing System

FDA 510(k) K233150 · Narang Medical , Ltd.

Substantially Equivalent

510(k) numberK233150

Submission

Device name
NET BRAND Osteosynthesis Nailing System
Applicant
Narang Medical , Ltd.
Delhi, IN
Received
September 27, 2023
Decision date
February 20, 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
JDS – Nail, Fixation, Bone
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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K241804TRIGEN INTERTAN 10S Nail SystemJDS · Traditional Smith & Nephew, Inc.08/22/2024SE
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
K111667Synthes Suprapatellar Insertion InstrumentsJDS · Special Synthes (Usa)12/05/2011SE

More from Synthes (Usa)

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K150561NET Brand Small Fragment and Large Fragment Osteosynthesis Plating System, NET Brand of…HRS · Traditional 11/25/2015SE

Questions and answers

When was NET BRAND Osteosynthesis Nailing System cleared by the FDA?

NET BRAND Osteosynthesis Nailing System (K233150) received a 510(k) decision of Substantially Equivalent on February 20, 2024, 146 days after the submission was received.

What is the product code of K233150?

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