← Product Code [GZT](/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GZT) · K960807

# TEW CRANIAL/SPINAL RETRACTOR MODEL A1090 (K960807)

_Ohio Medical Instrument Co., Inc. · GZT · May 17, 1996 · Neurology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GZT/K960807

## Device Facts

- **Applicant:** Ohio Medical Instrument Co., Inc.
- **Product Code:** [GZT](/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GZT.md)
- **Decision Date:** May 17, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 882.4800
- **Device Class:** Class 2
- **Review Panel:** Neurology
- **Attributes:** Therapeutic

## Indications for Use

The TEW Cranial/Spinal Retractor (A-1090) is designed for posterior fossa or intraspinal microsurgery where retraction is required.

## Device Story

TEW Cranial/Spinal Retractor is a self-retaining surgical retractor system used in neurosurgery. Device consists of a frame body with two independently movable arms and flexible micro-retractor arms for delicate neural tissue retraction. Operation involves rotating a worm gear with a hex wrench to translate an acme threaded shaft; worm/worm gear design provides self-locking mechanism. Blades can be pre-attached outside the wound using a formed locking edge to prevent detachment. Flexarm assemblies allow unrestricted placement along retractor arms for micro-retraction. Device provides stable, fixed-position retraction during microsurgical procedures, assisting surgeons in maintaining clear surgical fields.

## Clinical Evidence

Bench testing only.

## Technological Characteristics

Retractor frame body made of titanium; blades, micro-retractors, and flexarm assemblies made of stainless steel. Features two independently movable arms driven by a worm/worm gear mechanism and hex wrench. Self-locking design. Modular components include various blade types (curved, tapered, hooked, serrated) and flex arms of varying lengths.

## Regulatory Identification

A self-retaining retractor for neurosurgery is a self-locking device used to hold the edges of a wound open during neurosurgery.

## Predicate Devices

- Karlin Crank Frame Spinal Retractor Set
- Apfelbaum Cerebellar Retractor
- Budde® Halo Retractor

## Submission Summary (Full Text)

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>
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K960807

# II SUMMARY AND CERTIFICATION

Summary of Safety and Effectiveness TEW Cranial/Spinal Retractor™

Pursuant to Section 513(I) of the Federal Food, Drug and Cosmetics Act.

1. General Information:

Classification Name: Self-retaining retractor for neurosurgery

Common/Usual Name: Self-retaining Retractor

Proprietary Name: TEW Cranial/Spinal Retractor™

Applicant's Name and Address: F. William Sweet, Regulatory Affairs Manager
Ohio Medical Instrument Company, Inc. (OMI)
3924 Virginia Avenue.
Cincinnati, Ohio 45227

2. Name of predicate device(s):

Karlin Crank Frame Spinal Retractor Set

Apfelbaum Cerebellar Retractor

Budde® Halo Retractor - for blades, micro-retractors and flex arms

3. Classification:

Self-retaining retractor for neurosurgery are Class II (21CFR 882.4800).

4. Performance Standards:

No applicable performance standards have been established by FDA under section 514 of the Food, Drug and Cosmetic Act.

5. Intended Use and Device Description:

Intended Use: The TEW Cranial/Spinal Retractor (A-1090) is designed for posterior fossa or intraspinal microsurgery where retraction is required.

The TEW Cranial/Spinal Retractor is a combination of a frame retractor body for skin or muscle retraction and flexible micro-retractor arms for delicate neural tissue retraction.

Device Description: TEW Cranial/Spinal Retractor™ is made from titanium and the blades, micro-retractors and flexarm assemblies are made from stainless steel. It has two movable arms, which operate independently by rotating a worm on a worm gear thus allowing an acme threaded shaft to translate through the worm gear (Patent pending). The

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# II SUMMARY AND CERTIFICATION - Continued

## 5. Intended Use and Device Description: - Continued

mechanism of the TEW Retractor is self locking due to the worm/worm gear design. A hex wrench is used to drive the system.

TEW Retractor blades can be pre-attached to the arms outside of the wound and a formed locking edge on the blades prevent them from falling off. The blades can also be pre-positioned and once retraction has been initiated, blades will remain in a fixed position.

TEW Retractor micro-retraction is accomplished by unrestricted placement of the flexarm assemblies along the entire length of the retractor arms. There is no limit to the number of flexarms that can be used.

## Options:

A-1055 Tew Micro-Retractors
A-1057 Curved Blades
A-1071 Serrated TEW Micro Retractors
A-1074 Tapered Retractor Blade Set
A-1076 Hooked TEW Micro Retractors
4-38-A-1011 9" Flex Arm
4-38-A-1012 12" Flex Arm
4-38-A-1140 Halo Mini Vise Assembly

## 6. Summary of Substantial Equivalence:

Indications: The TEW Cranial/Spinal Retractor (A-1090) is designed for posterior fossa or intraspinal microsurgery where retraction is required.

Design: KARLIN Retractor crank frame has one movable arm, operated by rotating a pinion gear on a gear rack with a latch lock on the rack teeth. A square drive wrench is used to drive the system.

TEW Retractor has two movable arms, operating independently by rotating a worm on a worm gear allowing an acme threaded shaft to translate through the worm gear. The mechanism of the TEW Retractor is self locking due to the worm/worm gear design. A hex wrench is used to drive the system.

KARLIN Retractor blades are pre-positioned in the wound. The blades have no locking device to keep them from falling off the arms if blade attachment is performed outside of the wound.

TEW Retractor blades can be pre-attached to the arms outside of the wound and a formed locking edge on the blades prevent them from falling off. The blades can also be pre-positioned and once force is applied to them they will snap into place.

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# II SUMMARY AND CERTIFICATION - Continued

## 6. Summary of Substantial Equivalence - Continued

Blade configuration between the KARLIN and TEW is the same for the only blade that KARLIN offers with differences of width and height. TEW also has blades with points for anchoring to bone and another for soft tissue use.

TEW Retractor micro-retraction is accomplished by unrestricted placement of the flexarm assemblies along the entire length of the retractor arms. There is no limit to the number of flexarms that can be used. KARLIN Retractor has a self-retaining attachment to either retractor arm from which a single slide holder can be positioned along the arm length. Suction retractors are mounted in the slide holder and placed accordingly. The KARLIN attachment allows for two such retractors.

APFELBAUM Retractor, self-retaining retractor with 4x4 prongs. It has a pawl and gear rack lock system, similar to a rack and pinion gear lock, and two hexagonal posts fixed to each arm for flexarm attachment. Two flexarms can be used with the unit.

APFELBAUM Retractor uses the 4x4 prong for retaining tissue instead of separate blades capable of moving on a retractor arm system such as KARLIN or TEW. Three blades are available with the APFELBAUM unit for micro-retraction, one set being a left and right hand.

Materials: KARLIN Retractor, blades and self-retaining attachment is made from stainless steel.

TEW Retractor is titanium and the blades are stainless steel. TEW self-retaining flexarm assemblies are made from stainless steel.

APFELBAUM Retractor and blades are made from stainless steel and blades are malleable for soft tissue use.

Manufacturing: The manufacturing processes (milling, turning, wire cutting and forming) used in the TEW Cranial/Spinal Retractor™ are the same as those used in the predicate devices (Karlin Crank Frame Spinal Retractor and Apfelbaum Cerebellar Retractor).

Specifications: The specifications of the TEW Cranial/Spinal Retractor™ are the same as those of the predicate devices.

Conclusion: The indications, design, materials, manufacturing and specifications of the TEW Cranial/Spinal Retractor™ do not raise any new issues relating to safety and effectiveness.

OMI thus considers the TEW Cranial/Spinal Retractor™ to be equivalent to the predicate devices.

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**Source:** [https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GZT/K960807](https://fda.innolitics.com/submissions/NE/subpart-e%E2%80%94neurological-surgical-devices/GZT/K960807)

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