Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are indicated for the preparation of dental cavities for restorations, such as fillings.

Device Description

The Access™ L & KL and RotaMax™ L & KL Fiber Optic High Speed Dental Handpieces and Accessories are indicated for use in the preparation of dental cavities for restorations, such as fillings. These handpicces arc a scries of fiber optic high speed, air-driven turbine handpieces for use with standard size burs in accordance with ISO 1797. The technological characteristics and form/fit/function of the Access™ L & KL and RotaMax™ L & KL handpieces, respectively, are substantially equivalent to the Bien-Air Prestige L & LK Turbine Handpieces (FDA-cleared via K983183) and the Bora L & LK Turbine Handpieces (FDA-cleared via K983183).

The Access™4 series have a stainless steel ball bearing turbine with rotational speeds of up to 335,000 rpm and a smaller head as compared to the RotaMaxTM models. The Access™ is available for use with a Sable 6 Hole, 360° Swivel Quick Connect Coupler or Multiflex™ Coupler. The handpiece also contains a triple spray cooling system. The three air and water ports are located within the detachable diffuser. The diffuser is replaceable and is easily removed for cleaning. The Access™ incorporates an anti-retraction valve within the handle. The handpiece is autoclavable to 135° C. The Access™ has a patented nonheating, push button chuck bur-changing mechanism. The dual glass optics consist of a single block of optic rods. The glass rods are angled to help reduce shadows on the tooth. The fiber-optic light unit is fully interchangeable.

The RotaMax™ series have a ball bearing turbine with rotational speeds of up to 310,000 rpm and a larger head as compared to the Access™ models. The RotaMax™ is available for use with a Sable 6 Hole, 360° Swivel Quick Connect Coupler or Multiflex™ Coupler. The handpiece also contains a triple sprav cooling system. The three air and water ports are located within the detachable diffuser. The diffuser is replaceable and is easily removed for cleaning. The RotaMax™ incorporates an anti-retraction valve within the handle. The handpiece is autoclavable to 135° C. The RotaMax™ also has a patented nonheating, push button chuck bur-changing mechanism. The dual glass optics consist of a single block of optic rods. The glass rods are angled to help reduce shadows on the tooth. The fiber-optic light is fully interchangeable.

The electronic fiber optic control board available for use with the Access™ and RotaMax™ series handpieces is for one or two handpieces and supplies an adjustable power output ranging from 2 - 3.5 volts. The control board has an adjustable illumination time delay ranging from 0.5 - 4.5 seconds for each handpiece.

A range of air hoses are available for use with the Access™ and RotaMax™ series handpieces. The connectors for these hoses meet the criteria either for Type B or C per ISO 9168, and therefore have five outlets (to accommodate drive-air & exhaust, fiber optic, spray-air, and irrigation) or four outlets plus electrical contacts (to accommodate drive-air & exhaust, fiber optic power supply, sprayair, and irrigation). The air hoses arc straight and come in various colors.

KaVo Spray (preamendments device) or other FDA-cleared lubricants may be used to lubricate the Access™ L & KL and RotaMax™ L & KL Fiber Optic High Speed Dental Handpieces.

AI/ML Overview

The provided text is a 510(k) Summary for dental handpieces and accessories. It describes the device, its intended use, and substantial equivalence to predicate devices, but does not contain information about specific acceptance criteria or a study proving that the device meets those criteria in the way typically expected for an AI/ML device.

Instead, the document focuses on demonstrating substantial equivalence through conformity with established performance and safety standards for medical devices.

Therefore, for almost all the requested information, the answer will be "Not Applicable" or "Information Not Provided in Text".

Here's a breakdown of the requested information based on the provided text:

1. A table of acceptance criteria and the reported device performance

Acceptance Criteria	Reported Device Performance
Not Explicitly Stated as Numerical Acceptance Criteria	The device's performance is demonstrated through conformity with a range of ISO and IEC standards for medical devices. Explicit numerical performance metrics with defined acceptance thresholds are not provided.
Conformity to ISO 7785-1 (High-speed Air Turbine Handpieces)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to ISO 9168 (Dental Handpieces Hose Connections)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to ISO 1797-1 (Dental Rotary Instruments Shanks)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to ISO 11134 (Sterilization of health care products)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to ISO 10993 Part-1 (Biological Evaluation of Medical Devices)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to IEC 60601-1 (Medical Electrical Equipment Part 1: General requirements for safety)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."
Conformity to IEC 60601-1-2 (Medical Electrical Equipment Part 1: General requirements for safety - 2. Collateral Standard: Electromagnetic compatibility)	"Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device."

2. Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)

Sample Size: Not Applicable. The document does not describe a clinical "test set" in the context of an AI/ML development. The "performance and safety" assessment is based on conformity to engineering and medical device standards, which would involve testing according to those standards, but not a patient-data-based test set as typically understood for AI/ML.
Data Provenance: Not Applicable.

3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)

Not Applicable. This information is not relevant to the type of device (dental handpiece) and the type of evidence presented (conformity to standards, not AI/ML performance on clinical data).

4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

Not Applicable. This concept relates to expert review of clinical cases for ground truth establishment, which is not described.

5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

Not Applicable. The device is a dental handpiece, not an AI/ML diagnostic or assistive tool.

6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done

Not Applicable. This device is not an algorithm.

7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

Not Applicable. Ground truth as typically defined for AI/ML performance evaluation is not relevant here. The "ground truth" for this device's safety and effectiveness is its compliance with recognized industry standards for dental handpieces, sterilization, biocompatibility, and electrical safety.

8. The sample size for the training set

Not Applicable. This device is not an AI/ML model, so there is no training set.

9. How the ground truth for the training set was established

Not Applicable. This device is not an AI/ML model, so there is no training set or associated ground truth establishment process.

Summary

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510(k) SUMMARY OF SAFETY AND EFFECTIVENESS Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories

510(k) Summary Page 1 of 3

l. Submitter Information

510(k) Owner:	Sable Industries, Inc.100 Campbell Avenue, Suite 5Kitchener, Ontario N2H 4X8Canada	NOV 1 4 2007
Contact Person:	Jacob Jagt - QA Manager(519) 579-9323 (office)(519) 579-9324 (fax)
United States Agent/ U.S. Consultant:	Kevin Randall - PresidentGlobalReg Compliance Associates, Inc.581 Whiles CourtErie, CO 80516(303) 956-8595 (direct)(303) 828-0835 (fax)Email: kevin@globalregcompliance.com

Date Summary	September 4, 2007
Prepared:

II. Name of Device

Trade Name: Access™ L & KL and RotaMax™ L & KL Fiber Optic High . Speed Dental Handpieces & Accessories
Common Name: Fiber Optic High Speed Dental Handpieces & Accessories .
Classification Name: Handpiece, Air-Powered, Dental .

III. Predicate Devices

Subject Device	Predicate Device(s)
Access™ L & KL Fiber Optic HighSpeed Dental Handpiece	Bien-Air Prestige L & LK TurbineHandpiece (K983183)
RotaMax™ L & KL Fiber Optic HighSpeed Dental Handpiece	Bien-Air Bora L & LK TurbineHandpiece (K983183)

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510(k) SUMMARY OF SAFETY AND EFFECTIVENESS Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories

510(k) Summary Page 2 of 3

IV. Device Description & Technological Characteristics

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510(k) SUMMARY OF SAFETY AND EFFECTIVENESS Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories

510(k) Summary Page 3 of 3

KaVo Spray (preamendments device) or other FDA-cleared lubricants may be used to lubricate the Access™ L & KL and RotaMax™ L & KL Fiber Optic High Speed Dental Handpieces.

Intended Use V.

Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are indicated for the preparation of dental cavities for restorations, such as fillings.

Non-Clinical Performance/Safety Data VI.

The performance and safety of the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are based upon conformity with applicable aspects of the following standards:

ISO 7785-1 High-speed Air Turbine Handpieces .
ISO 9168 Dental Handpieces Hose Connections ↓
ISO 1797-1 Dental Rotary Instruments Shanks .
ISO 11134 Sterilization of health care products Requirements . for validation and routine control - Industrial moist heat sterilization
ISO 10993 Biological Evaluation of Medical Devices Part-1: . Evaluation and Testing
IEC 60601-1 Medical Electrical Equipment Part 1: General . requirements for safety
IEC 60601-1-2 Medical Electrical Equipment Part 1: General . requirements for safety - 2. Collateral Standard: Electromagnetic compatibility - Requirements and test.

Conformity with the above standards demonstrates that the Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are as safe, as effective, and perform as well as or better than the predicate device.

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Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a circular seal with the words "DEPARTMENT OF HEALTH AND HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized symbol of three human figures connected by flowing lines.

Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850

NOV 1 4 2007

Sable Industries, Incorporated C/O Mr. Kevin Randall President GlobalReg Compliance Associates, Incorporated 581 Whiles Court Erie, Colorado 80516

Re: K072554

Trade/Device Name: Fiber Optic High Speed Dental Handpieces & Accessories Regulation Number: 872.4200 Regulation Name: Dental Handpiece and Accessories Regulatory Class: I Product Code: EFB Dated: September 4, 2007 Received: September 10, 2007

Dear Mr. Randall:

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 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. Randall

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 (240) 276-0115. 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 (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.

Sincerely yours.

Neil R. P. Oden

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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Page of

510(k) Number (if known): K027554

Device Name:

Fiber Optic High Speed Dental Handpieces & Accessories

Indications For Use:

Sable Industries Fiber Optic High Speed Dental Handpieces & Accessories are indicated for the preparation of dental cavities for restorations, such as fillings.

PLEASE DO NOT WRITE BELOW THIS LINE CONTINUE ON ANOTHER PAGE IF NEEDED

Concurrence of CDRH, Office of Device Evaluation (ODE)

Prescription Use X

Susan Rianon

-sizn Sign-Off) rion of Anesthesiology, General Hospital, address control. Dental Devices

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Over-The-Counter Use

(Optional Format 1-2-96)

xiv

Regulation Number and Section

§ 872.4200 Dental handpiece and accessories.

(a)
Identification. A dental handpiece and accessories is an AC-powered, water-powered, air-powered, or belt-driven, hand-held device that may include a foot controller for regulation of speed and direction of rotation or a contra-angle attachment for difficult to reach areas intended to prepare dental cavities for restorations, such as fillings, and for cleaning teeth.(b)
Classification. Class I.