SYNTHES CARNIOFACIAL PLATE AND SCREW SYSTEM

K050608 · Synthes (Usa) · JEY · May 18, 2005 · Dental

Device Facts

• Record ID: K050608
• Device Name: SYNTHES CARNIOFACIAL PLATE AND SCREW SYSTEM
• Applicant: Synthes (Usa)
• Product Code: JEY · Dental
• Decision Date: May 18, 2005
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 872.4760
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

Synthes Craniofacial Plate and Screw System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and selective orthognathic surgery of the maxilla and chin.

Device Story

Synthes Craniofacial Plate and Screw System consists of titanium or titanium alloy plates and meshes of various shapes/sizes; designed for internal bone fixation. System utilizes 1.8 mm screws and 2.1 mm emergency screws; installed using 1.8 mm hexagonal screwdriver blades. Intended for single use in clinical settings by surgeons for midface/craniofacial trauma, reconstruction, and orthognathic procedures. Provides mechanical stabilization of bone segments to facilitate healing and structural restoration.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Materials: Titanium or titanium alloy. Components: Plates, meshes, 1.8 mm screws, 2.1 mm emergency screws. Instrumentation: 1.8 mm hexagonal screwdriver blades. Single-use only.

Indications for Use

Indicated for patients requiring internal fixation for selective trauma of the midface and craniofacial skeleton, craniofacial surgery, reconstructive procedures, and selective orthognathic surgery of the maxilla and chin.

Regulatory Classification

Identification

A bone plate is a metal device intended to stabilize fractured bone structures in the oral cavity. The bone segments are attached to the plate with screws to prevent movement of the segments.

Predicate Devices

• Synthes Midfacial System
• Synthes Orbital Mesh Plates F/Synthes Midfacial System
• Synthes Maxillofacial Titanium Micro Set
• Synthes Cranial Plates
• Synthes 1.5 mm Self-tapping cortex screws

Submission Summary (Full Text)

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K050608

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510(k) Summary 3.0

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| Sponsor: | Synthes (USA)<br>1302 Wrights Lane East<br>West Chester, PA 19380<br>[phone] |
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| Device Name: | Synthes (USA) Craniofacial Plate and Screw System |
| Classification: | Class II, 21 CFR §872.4760<br>Bone plate |
| | Class II, 21 CFR §872.4880<br>Intraosseous fixation screw or wire |
| Predicate Device: | Synthes Midfacial System<br>Synthes Orbital Mesh Plates F/Synthes Midfacial System<br>Synthes Maxillofacial Titanium Micro Set<br>Synthes Cranial Plates<br>Synthes 1.5 mm Self-tapping cortex screws |
| Device Description: | Synthes Craniofacial Plate and Screw System consist of plates and<br>meshes that come in a variety of shapes and sizes to meet the<br>anatomical needs of the patient. This system is designed for use<br>with 1.8 mm screws and 2.1 mm emergency screws. The screws<br>will be used with Synthes 1.8 mm hexagonal screwdriver blades.<br>System components are manufactured in either titanium or titanium<br>alloy and are intended for single use only. |
| Intended Use: | Synthes Craniofacial Plate and Screw System is intended for use in<br>selective trauma of the midface and craniofacial skeleton;<br>craniofacial surgery; reconstructive procedures; and selective<br>orthognathic surgery of the maxilla and chin. |
| Substantial<br>Equivalence: | Documentation is provided which demonstrates that the Synthes<br>Craniofacial Plate and Screw System is substantially equivalent to<br>other legally marketed devices. |

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Image /page/1/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized depiction of an eagle or bird-like figure with three wing-like shapes. The text "DEPARTMENT OF HEALTH AND HUMAN SERVICES - USA" is arranged in a circular pattern around the emblem.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

## MAY 1 8 2005

Ms. Sheri L. Musgnung Senior Regulatory Affairs Specialist Synthes (USA) 1302 Wrights Lane East West Chester, Pennsylvania 19380

Re: K050608

Trade/Device Name: Synthes (USA) Craniofacial Plate and Screw Systems Regulation Number: 872.4760 Regulation Name: Bone Plate Regulatory Class: II Product Code: JEY, DZL Dated: March 9, 2005 Received: March 10, 2005

Dear Ms. Musgnung:

We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting (111), and be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Eederal Register.

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Page 2 - Ms. Musgnung

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number [phone] or [phone] or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours,

Chiu-Lin, Ph.D.

Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known):

Device Name:

Indications:

Kosopor

Synthes (USA) Craniofacial Plate and Screw System

Synthes Craniofacial Plate and Screw System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and selective orthognathic surgery of the maxilla and chin.

Prescription Use X (Per 21 CFR 801 Subpart D) AND/OR

Over-The-Counter Use (21 CFR 807 Subpart C)

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Concurrence of CDRH, Office of Device Evaluation (ODE)

Susan Russe

15000

(Division Sign-Off) (Division Sign-On)
Division of Anesthesiology, General Hospital, Intection Control, Dental Devices

510(k) Number.__

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