(293 days)
KV-1, K#940776, K#980216, K#921748, K#902836, K#932997
Not Found
No
The device description and intended use describe a purely mechanical/pneumatic system for air abrasion. There is no mention of AI, ML, image processing, or data analysis that would indicate the use of such technologies.
No.
The device is used for mechanical procedures like cavity preparation and removal of tooth structure, not for treating a disease or condition in a therapeutic sense.
No
The device description and intended use clearly state that it is used for "cavity preparation," "removal of tooth structure and restorative dental materials," and "site preparation" using "pressurized air and abrasive powder." These are all therapeutic or preparatory procedures, not diagnostic ones.
No
The device description clearly states it is a pneumatic device that combines pressurized air and abrasive powder delivered via a handpiece, indicating it is a hardware-based medical device.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information about a person's health. This testing is done outside of the body (in vitro).
- Device Function: The S.S. White Technologies 6500 Series Air Abrasion Devices are used directly on the tooth structure for physical procedures like cavity preparation and material removal. They do not analyze biological specimens.
The device description and intended use clearly indicate it's a tool for performing dental procedures in vivo (within the living body), not for diagnostic testing of samples in vitro.
N/A
Intended Use / Indications for Use
The S.S. White Technologies 6500 Series Air Abrasion Devices are used for cavity preparation in Classes I, II, III, IV, and V. The uses include removal of tooth structure and restorative dental materials, and site preparation for pit and fissure sealant therapy and bonding of porcelain and ceramic. They are also used for restoration prophylaxis.
Product codes
KOJ
Device Description
The 6500-D, 6500-E, and 6500-F are pneumatic devices which combine pressurized air and abrasive powder (e.g. aluminum oxide or sodium bicarbonate) to produce a high velocity stream of particles to perform dental restorative procedures. The abrasive particulate is delivered via a small handpiece which is approximately the size of a dental drill handpiece. The systems are designed for ease of service and maintenance with a readily accessible refillable container for the particulate supply.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
KV-1, K#940776, Mach Series, K#980216, K#921748, Microetcher, K#902836, MicroPrep Cavity Preparation System, K#932997
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc)
Not Found
§ 872.6080 Airbrush.
(a)
Identification. An airbrush is an AC-powered device intended for use in conjunction with articulation paper. The device uses air-driven particles to roughen the surfaces of dental restorations. Uneven areas of the restorations are then identified by use of articulation paper.(b)
Classification. Class II. The special control for this device is International Electrotechnical Commission's IEC 60601-1-AM2 (1995-03), Amendment 2, “Medical Electrical Equipment—Part 1: General Requirements for Safety.”
0
3/8/99
510(k) Summary
Company Name: S.S. White Technology, Inc. 151 Old New Brunswick Road Piscataway, NJ 08854
Company Contact, Regulatory Affairs: Dave Taylor S.S. White Technology, Inc. 151 Old New Brunswick Road Piscataway, NJ 08854 Phone: (732) 752-8300 ext 390 Fax: (732) 752-0698 E-mail: dataylor@gateway.net
Device Name:
6500 Series Air Abrasion Systems
Predicate Devices:
KV-1, K#940776 (Kreativ, San Diego, CA), Mach Series, K#980216 (Kreativ, San Diego, CA), K#921748 (American Dental Technologies, Troy, MI), Microetcher, K#902836 (Danville Engineering) and the MicroPrep Cavity Preparation System, K#932997 (Sunrise Technologies, Inc.)
Device and Indications for Use:
The 6500-D, 6500-E, and 6500-F are pneumatic devices which combine pressurized air and abrasive powder (e.g. aluminum oxide or sodium bicarbonate) to produce a high velocity stream of particles to perform dental restorative procedures. The abrasive particulate is delivered via a small handpiece which is approximately the size of a dental drill handpiece. The systems are designed for ease of service and maintenance with a readily accessible refillable container for the particulate supply.
The 6500-D, 6500-E, and 6500-F are used for cavity preparation in Classes I, II, III, IV, and V. The uses include removal of tooth structure and restorative dental materials, and site preparation for pit and fissure sealant therapy and bonding of porcelain and ceramic. They are also used for restoration prophylaxis.
Discussion:
Since the intended use and technical specifications of the 6500-D, 6500-E, and 6500-F are virtually identical to the predicate devices, and the differences in the devices only serve to make them marketable, we believe the 6500 Series devices are substantially equivalent to the predicate devices and can be marketed under section 510(k) of the FD & C Act.
1
Public Health Service
Image /page/1/Picture/2 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular emblem with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the top half of the circle. Inside the circle is a stylized image of an eagle with three lines representing its wings and head.
SEP 2 9 1999
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
.
Mr. Dave Taylor S.S. White Technologies, Incorporated 151 Old New Brunswick Road Piscataway, New Jersey 08854-3761
K984415 Re : S.S. White Technologies, Models 6500-D, Trade Name: 6500-E, and 6500-F Requlatory Class: İII Product Code: KOJ Dated: November 26, 1998 December 10, 1998 Received:
Dear Mr. Taylor:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act 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 (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. ಗಳ substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
2
Page 2 - Mr. Taylor
This letter will allow you to begin marketing your device as described in your 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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact Also, please note the Office of Compliance at (301) 594-4639. the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours
Timothy A. Ulatowski
Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications Statement
510(k) submission: S.S. White Technologies 6500 Series Air Abrasion Devices
Indications for Use:
The S.S. White Technologies 6500 Series Air Abrasion Devices are used for cavity preparation in Classes I, II, III, IV, and V. The uses include removal of tooth structure and restorative dental materials, and site preparation for pit and fissure sealant therapy and bonding of porcelain and ceramic. They are also used for restoration prophylaxis.
Susan Runno
(Division Sign-Off) Division of Dental, Infection Control, and General Hospital Devices 24,2441 510(k) Number
- PRESCRIPTION
DEVICE