← Product Code [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB) · K962552

# EZ-6 PROXIMAL HUMERAL INTERAMEDULLARY ROD SYSTEM (K962552)

_Biodynamic Technologies, Inc. · HSB · Sep 25, 1996 · Orthopedic · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K962552

## Device Facts

- **Applicant:** Biodynamic Technologies, Inc.
- **Product Code:** [HSB](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB.md)
- **Decision Date:** Sep 25, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 888.3020
- **Device Class:** Class 2
- **Review Panel:** Orthopedic
- **Attributes:** Therapeutic

## Intended Use

The EZ-Fix™ Proximal Humeral Intramedullary Rod is an internal skeletal fixation device indicated for intramedullary use to stabilize fractures of the proximal humerus.

## Device Story

EZ-Fix™ Proximal Humeral Intramedullary Rod is an internal skeletal fixation device for stabilizing proximal humeral fractures. The device is a cylindrical titanium alloy (TI-6AL-4V) rod available in 9mm, 11mm, 13mm, and 15mm diameters. It features four proximal screw holes for humeral head fragment stabilization, including a 6.5mm cannulated screw hole and 5mm bone screw holes. The rod is tri-slotted distally to accommodate anatomical variances and includes shallow grooves for flexibility and rotational stability. An insertion/extraction hole is protected by a titanium capscrew to prevent soft tissue ingrowth. The device is implanted by a surgeon in a clinical setting; it does not require reaming. The rod provides mechanical stabilization of the fracture site to facilitate healing.

## Clinical Evidence

Bench testing only. Mechanical testing was conducted by the University of Miami Biomechanics Laboratory at Mount Sinai using ASTM F383 standards for intramedullary rods. Results confirmed the device design is sound and performance values are equivalent to the referenced predicate devices.

## Technological Characteristics

Material: Titanium alloy (TI-6AL-4V). Geometry: Cylindrical rod, 9-15mm diameter, 155mm length, tri-slotted distal end. Fixation: Proximal screw holes (6.5mm and 5mm screws) and suture holes. Sterilization: Gamma radiation (SAL 10^-6) or steam autoclave (SAL 10^-4). Standards: ASTM F383, ANSI/AAMI/ISO 11137-1994.

## Regulatory Identification

An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.

## Predicate Devices

- Orthologic® OrthoNail® Humeral Intramedullary Fixation Device
- Acumed™ Polarus® Proximal Humeral Fixation System
- Applied Osteo Systems True/Flex™ Fixation Device
- Howmedica Seidel™ Humeral Locking Nail System

## Submission Summary (Full Text)

> This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com.
>
> Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/).

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K962552
SEP 25 1996

# Section 510(k) Premarket Notification

## Summary of Safety and Effectiveness Information

Regulatory Authority: Safe Medical Devices Act of 1990, 21 CFR 807.92

**Device Trade Name:** EZ-Fix™ Proximal Humeral Intramedullary Rod System
**Common Name:** Intramedullary Rods
**Registration Number:** 888.3020
**Classification Name:** Rod, Fixation, Intramedullary and Accessories

## Establishment Name &amp; Registration Number:

**Name:** Biodynamic Technologies, Inc.
East Newport Center Drive
Deerfield Beach, Florida 33442
(305) 421-3166 (305) 570-6368 FAX

**Number:** 1035157

## Contact Person:

Danny Hodgeman
Biodynamic Technologies, Inc.
East Newport Center Drive
Deerfield Beach, Florida 33442
(305) 421-3166 (305) 570-6368 FAX

## Classification:

**Device Class:** Class II
**Classification Panel:** Orthopedic

## Special Controls:

Not applicable to this device.

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# Device Description:

The EZ-Fix™ Proximal Humeral Intramedullary Rod is an internal skeletal fixation device indicated for intramedullary use to stabilize fractures of the proximal humerus. The device has been engineered for ease of use and the ability to accommodate a wide variety of proximal humeral fractures.

The EZ-Fix™ Humeral Rod is cylindrical and available in 9mm, 11mm, 13mm and 15mm diameters and is approximately 155mm in length. Proximally there are four screw holes for capturing and stabilizing humeral head fragments. Most proximally, the EZ-Fix™ Humeral Rod accepts a 6.5mm cannulated screw. Two holes, one 60 degrees anterior and one 60 degrees posterior from the lateral side, accept 5mm bone screws. The most distal hole also accepts a 5mm bone screw and is aligned laterally with the most proximal screw hole.

In addition to the four proximal holes in the 11mm, 13mm and 15mm rods, there are four suture holes proximally to attach soft tissues.

The EZ-Fix™ Humeral Rod is tri-slotted distally allowing the rod to collapse and accommodate anatomical variances. These three slots are of different lengths and extend from the distal end of the rod to just below the four proximal screw holes.

The EZ-Fix™ Humeral Rod has shallow grooves situated below the screw holes and extending lengthwise for ease of implantation without reaming, enhanced flexibility and rotational stability.

An insertion/extraction instrumentation attachment hole is located in the proximal end of the rod. This threaded hole is protected by a titanium alloy (TI-6AL-4V) capscrew, disallowing soft tissue ingrowth post implantation.

The EZ-Fix™ Humeral Rod is titanium alloy (TI-6AL-4V) for biocompatibility and strength.

# Substantially Equivalent Devices:

Orthologic® OrthoNail® Humeral Intramedullary Fixation Device

Acumed™ Polarus® Proximal Humeral Fixation System

Applied Osteo Systems True/Flex™ Fixation Device.

Howmedica Seidel™ Humeral Locking Nail System

# Comparison to Predicate Device:

The EZ-Fix™ Humeral Rod is substantially equivalent to the OrthoNail®, the Polarus®, and the True/Flex™ in that it is manufactured from titanium or titanium alloy. Like the OrthoNail®, the Polarus®, and the Seidel™, the EZ-Fix™ is of a cylindrical configuration proximally.

The EZ-Fix™ is indicated for proximal humeral fractures as is the OrthoNail®, the Polarus®, and the Seidel™. Like the OrthoNail®, the Polarus®, and the Seidel™, the

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EZ-Fix™ has screw holes for fixation. In addition, the EZ-Fix™ has suture holes proximal like the OrthoNail®.

The EZ-Fix™ is equivalent to the True/Flex™ in that reaming is not required and neither devices are cannulated. Like the OrthoNail®, the EZ-Fix™ threaded insertion/extraction hole is protected by a titanium alloy capscrew, disallowing soft tissue ingrowth post implantation.

## Packaging:

### Sterile

The EZ-Fix™ Proximal Humeral Intramedullary Rods are packaged in a blister package consisting of a thermoformed inner tray that contains the EZ-Fix™ Rod. This tray is protected by an outer thermoformed tray that is sealed by TYVEK CR-27. The outer TYVEK cover is labeled and has affixed to it the Patient Chart Labels. Both the inner and outer trays when sealed with the TYVEK cover are enclosed in a box that is sealed and indicates the sterility of the contents. Packaging material consists of .025 BT/CTD PETG, WEB#1:CTD 1073B TYVEK CR-27.

### Non-Sterile

The EZ-Fix™ Proximal Humeral Intramedullary Rod System includes EZ-Fix™ humeral rods and instrumentation and is made available non-sterile. Steam autoclavable sterilization trays have been designed to contain the EZ-Fix™ Rod System and maintain adequate separation of the implants and instruments. Sterilization cycles should be followed appropriately to achieve a 10⁻⁶ sterility assurance level (SAL).

## Sterilization / Re-sterilization:

### Sterile

- The EZ-Fix™ Proximal Humeral Intramedullary Rod may be supplied sterile.
- Sterilization is achieved by means of gamma radiation.
- Sterilization complies with ANSI/AAMI/ISO 11137-1994 practices.
- 10% of each production lot of EZ-Fix™ kits are tested (6% for bacteriostasis - fungistasis studies and 4% for bioburden recovery determination)
- The EZ-Fix™ is packaged in a blister package consisting of a thermoformed inner tray that contains the EZ-Fix™ Rod. This tray is protected by an outer thermoformed tray that is sealed by TYVEK CR-27. The outer TYVEK cover is labeled and has affixed to it the Patient Chart Labels. Both the inner and outer trays when sealed with the TYVEK cover are enclosed in a box that is sealed and indicates the sterility of the contents. Packaging material consists of .025 BT/CTD PETG, WEB#1:CTD 1073B TYVEK CR-27.
- The radiation dose is based on the ANSI/AAMI/ISO 11137.1994 dose setting.
- Sterilization Assurance Level (SAL) is 10⁻⁶.
- Sterilization process used is Cobalt 60.
- The EZ-Fix™ is non-pyrogenic. Pyrogenicity testing of the EZ-Fix™ to determine level of endotoxin performed using LAL (Limulus Amebocyte Lysate) method.

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## Non-Sterile

- The EZ-Fix™ Humeral Intramedullary Rods and all instrumentation may be supplied non-sterile.
- Steam autoclavable sterilization trays have been designed to contain the EZ-Fix™ Rod System and maintain adequate separation of the implants and instruments.
- Sterilization cycles should be followed appropriately to achieve a 10⁻⁴ sterility assurance level (SAL).
- See Appendix I for Sterilization Procedure
- The EZ-Fix™ is non-pyrogenic. Pyrogenicity testing of the EZ-Fix™ to determine level of endotoxin performed using LAL (Limulus Amebocyte Lysate) method.

## Testing:

The EZ-Fix™ Proximal Humeral IM Rod has been tested by the University of Miami Biomechanics Laboratory at Mount Sinai in Miami Beach, Florida, based upon ASTM test standards for intermedullary rods (F383). Test results proved the rods to be of sound design.

## Equivalence:

These test values are identical to those obtained on the referenced equivalent.

## Conclusion:

Based on the materials, intended uses, design, testing, and manufacturing, the EZ Fix™ Proximal Humeral Intramedullary Rod System is equivalent to the referenced legally marketed comparison devices. The feature comparison chart below graphically demonstrates equivalence.

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Comparison Table:

|  EZ-Fix™ | OrthoNall® | Polarus® | True/Flex™ | Seidel™ | Substantial Equivalence  |
| --- | --- | --- | --- | --- | --- |
|  Materials  |   |   |   |   |   |
|  Titanium Alloy | Titanium Alloy | Titanium | Titanium Alloy | Stainless Steel | Yes  |
|  Geometry  |   |   |   |   |   |
|  Cylindrical | Cylindrical/Flat | Cylindrical | Star Shaped | Cylindrical | Yes  |
|  Intended Use  |   |   |   |   |   |
|  Single Use | Single Use | Single Use | Single Use | Single Use | Yes  |
|  Proximal | Prox/Distal | Proximal | Mid/Distal | Prox/Mid Shaft |   |
|  Humeral | Humeral | Humeral | Humeral | Humeral |   |
|  Fractures | Fractures | Fractures | Fractures | Fractures |   |
|  Performance Standards  |   |   |   |   |   |
|  ASTM | ASTM | ASTM | ASTM | ASTM | Yes  |
|  Fixation  |   |   |   |   |   |
|  Interference | Interference | Interference | Interference | Interference | Yes  |
|  Optional | Optional | Optional | Mechanism | Mechanism |   |
|  Screw Holes | Screw Holes | Screw Holes |  |  |   |
|  Preparation (Reaming)  |   |   |   |   |   |
|  Optional | Yes | Yes | No | Yes | Yes  |
|  Cannulated  |   |   |   |   |   |
|  No | Yes | Yes | No | Yes | Yes  |
|  Sterile  |   |   |   |   |   |
|  Sterile | Non-Sterile | Sterile | Sterile | Sterile | Yes  |
|  Non-Sterile |  |  |  |  |   |

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**Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K962552](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/HSB/K962552)

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