EZ-6 Proximal Humeral Interamedullary Rod System

FDA 510(k) K962552 · Biodynamic Technologies, Inc.

Substantially Equivalent

510(k) numberK962552

Submission

Device name
EZ-6 Proximal Humeral Interamedullary Rod System
Applicant
Biodynamic Technologies, Inc.
Deerfield Beach, FL, US
Received
July 1, 1996
Decision date
September 25, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSB – Rod, Fixation, Intramedullary And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3020
Specialty
Orthopedic
Implant
Yes

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More from Fusion Orthopedics USA, LLC

510(k)DeviceDecision
K990436Ultimax Trochanteric Intramedullary Rod SystemHSB · Traditional 03/31/1999SE
K990513Ultimax Cortical Bone ScrewsHWC · Traditional 03/17/1999SE
K990481Ultimax Distal Radial (Volar) Locking Plate SystemHRS · Traditional 03/17/1999SE
K981230Ultimax Distal Femoral Intramedullary Rod SystemHSB · Traditional 06/01/1998SE
K980102Bti Humeral Intramedullary Rod SystemHSB · Traditional 04/03/1998SE
K974756Bti Large (7.0MM) Cannulated Transfixing ScrewsHWC · Traditional 03/12/1998SN
K972403Bti Cortical Bone ScrewsHWC · Traditional 08/29/1997SE
K970897Bti Distal Femoral Intramedullary Rod SystemHSB · Traditional 04/21/1997SE
K962706Ez-Fix Cannulated Screw SystemHWC · Traditional 11/13/1996SE
K962987Ez-Fix Small Cannulated Screw SystemHWC · Traditional 11/04/1996SE

Questions and answers

When was EZ-6 Proximal Humeral Interamedullary Rod System cleared by the FDA?

EZ-6 Proximal Humeral Interamedullary Rod System (K962552) received a 510(k) decision of Substantially Equivalent on September 25, 1996, 86 days after the submission was received.

What is the product code of K962552?

The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.