VITABLOCS

K102128 · Vita Zahnfabrik H.Rauter GmbH & Co. · EIH · Aug 11, 2010 · Dental

Device Facts

• Record ID: K102128
• Device Name: VITABLOCS
• Applicant: Vita Zahnfabrik H.Rauter GmbH & Co.
• Product Code: EIH · Dental
• Decision Date: Aug 11, 2010
• Decision: SESE
• Submission Type: Abbreviated
• Regulation: 21 CFR 872.6660
• Device Class: Class 2
• Attributes: Therapeutic, 3rd-Party Reviewed

Intended Use

Vitablocs® are indicated for use as a dental restoration including inlays, onlays, veneers, crowns and bridges. For use by or on the order of a dental professional such as DDS or DMD. Not for use. by the general public or OTC.

Device Story

Vitablocs are dental restorative materials used by dentists to fabricate inlays, onlays, veneers, crowns, and bridges. The device serves as a porcelain-based material for clinical dental restoration. It is intended for professional use only, requiring a prescription. The device is used in a clinical dental setting to restore tooth structure or function. It provides a durable material for dental prosthetics, benefiting patients by replacing damaged or missing tooth structure.

Clinical Evidence

No clinical data provided; bench testing only.

Technological Characteristics

Porcelain powder for clinical use. Classified under 21 CFR 872.6660, Product Code EIH. Class II device.

Indications for Use

Indicated for dental restorations including inlays, onlays, veneers, crowns, and bridges. For use by dental professionals (DDS/DMD) only; not for OTC use.

Regulatory Classification

Identification

Porcelain powder for clinical use is a device consisting of a mixture of kaolin, felspar, quartz, or other substances intended for use in the production of artificial teeth in fixed or removable dentures, of jacket crowns, facings, and veneers. The device is used in prosthetic dentistry by heating the powder mixture to a high temperature in an oven to produce a hard prosthesis with a glass-like finish.

Submission Summary (Full Text)

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Image /page/0/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo consists of a stylized eagle with three lines forming its body and wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged in a circular fashion around the eagle.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002

Vita Zahnfabrik H. Rauter GmbH & Company C/O Mr. Daniel W. Lehtonen Responsible Third Party Official Intertek Testing Services 2307 East Aurora Road, Unit B7 Twinsburg, Ohio 44807

AUG 1 1 2010

Re: K102128

Trade/Device Name: Vitablocs® Regulation Number: 21 CFR 872.6660 Regulation Name: Porcelain Powder for Clinical Use Regulatory Class: II Product Code: EIH Dated: July 27, 2010 Received: July 29, 2010

Dear Mr. Lehtonen:

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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can 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 Federal Register.

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Page 2- Mr. Lehtonen

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 on aves not 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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices /ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding of received of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportalProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

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/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely vours.

h For

Anthony D. Watson, B.S., M.S., M.B.A. 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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K102128

## Indications for Use

## 510(k) Number (if known):

AUG 1 1 2010

Device Name: Vitablocs® Indications for Use:

Vitablocs® are indicated for use as a dental restoration including inlays, onlays, veneers, crowns and bridges.

For use by or on the order of a dental professional such as DDS or DMD. Not for use. by the general public or OTC.

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

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

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Concurrence of CDRH, Office of Device Evaluation (ODE)

Kein Mulvey for MSR
(Division Sign Off)

Division of Dental, Infection Controlland General Hospital Devices 02128

510(k) Number

Prescription Use (Par. 21 CFR 801.109 OR

Over-The-Counter Use

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