← Product Code [MUH](/submissions/DE/subpart-b%E2%80%94diagnostic-devices/MUH) · K091866 # PROGENY VANTAGE PANORAMIC X-RAY SYSTEM (K091866) _Midmark · MUH · Jul 20, 2009 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/MUH/K091866 ## Device Facts - **Applicant:** Midmark - **Product Code:** [MUH](/submissions/DE/subpart-b%E2%80%94diagnostic-devices/MUH.md) - **Decision Date:** Jul 20, 2009 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.1800 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** 3rd-Party Reviewed ## Indications for Use The indications for use of the Progeny Vantage Extra-Oral Panoramic X-Ray System is to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. ## Device Story Progeny Vantage is an extraoral radiographic imaging system producing digital panoramic radiographs of teeth, jaw, and oral structures. System components include an X-ray tubehead with integrated collimation, digital image receptor, rotating C-arm, overhead arm, elevating column, patient positioning table, electronic control unit, and computer display workstation. Operated by dental professionals in a clinical setting using a deadman exposure switch. The device captures X-ray projections, which are converted to digital images for display on a monitor. It supports panoramic, TMJ, and ortho image profiles. The system aids clinicians in diagnosing oral diseases by providing high-resolution radiographic views. Image management, manipulation, and archiving are performed by external software not included with this device. ## Clinical Evidence Bench testing only. No clinical data provided. Safety and effectiveness were established through performance testing, verification against product specifications, software design validation, and hazard/risk assessment. ## Technological Characteristics Extraoral X-ray system; 60-84 kVp; 4-10 mA; 0.5mm² focal spot; digital sensor (96µm pixel size). Construction: aluminum castings with plastic and metal covers. Features telescoping column, rotating C-arm, and color touch screen interface. Operates via deadman switch. Connectivity: digital output to external workstation. Software performs image acquisition and control. ## Regulatory Identification An extraoral source x-ray system is an AC-powered device that produces x-rays and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. The x-ray source (a tube) is located outside the mouth. This generic type of device may include patient and equipment supports and component parts. ## Predicate Devices - Planmeca Promax ([K011619](/device/K011619.md)) - Instrumentarium Orthopantomograph OP100D ([K992385](/device/K992385.md)) - Gendex Orthoralix 8500 ([K050255](/device/K050255.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K091866 Progeny ## SECTION 7 Proprietary and Confidential ## 510(k) Summary as required by CFR section 807.92(c) JUL 2.0 2009 ## I. General Information - June 4, 2009 Date: Midmark Applicant: 675 Heathrow Dr. Lincolnshire, Ill. ୧୦୦୧୨ Contact Person: Alan Krema - 847-415-9800 x785 Telephone: - 847-415-9801 Fax: ## II. Names Device Name: | Trade Name: | Progeny Vantage Panoramic X-Ray System | |----------------------|------------------------------------------| | Common Name: | Panoramic X-Ray System | | Classification Name: | MUH - Unit, X-Ray, Extra oral with Timer | ## III. Predicate Devices | #K011619 | Planmeca Promax | |----------|------------------------------------------| | #K992385 | Instrumentarium Orthopantomograph OP100D | | #K050255 | Gendex Orthoralix 8500 | ## Product Description The Progeny Vantage Panoramic X-ray System is an extraoral radiographic imaging system for producing digital radiographs in a panoramic view of the teeth, jaw, and oral structure. {1}------------------------------------------------ The Progeny Vantage Panoramic Extraoral Radiographic Imaging System consists of the following main components: X-ray tubehead with integrated collimation. Digital Image Receptor Rotating C-Arm for tubehead and image receptor mounting Overhead arm Elevating Column Patient Positioning Table Electronic Control Unit Computer Display Workstation 8 ft. coil cord with exposure switch Optional Components: None ## V. Indications for Use / Rationale for Substantial Equivalence Indications For Use of the Progeny Vantage Panoramic X-Ray System: The indications for use of the Progeny Vantage Panoramic Extra Oral X-Ray System is to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. As a digital device, the images are displayed on a monitor. The Image management software, including any image manipulation, archiving, and communication are not a part of this device. The Vantage shares the same indications for use, materials, design, operational and functional features and is therefore substantially equivalent to the predicate devices listed in section III of this summary. The Progeny Panoramic Radiographic Imaging System is similar in design, composition, and function to the following devices introduced into commercial distribution after May 28, 1976: | #K011619 | Planmeca Promax | |----------|------------------------------------------| | #K992385 | Instrumentarium Orthopantomograph OP100D | | #K050255 | Gendex Orthoralix 8500 | Labeling for the currently marketed devices is included as Appendix B. Comparison Table {2}------------------------------------------------ | Characteristic | PlanMeca
Promax | Gendex
8500 | Instrumentarium
OP200D | Progeny
Vantage | |------------------------------|----------------------------------------------------------|-----------------------------------------------|----------------------------------------------------------|----------------------------------------------------------| | kVp | 60-84 kVp | 60-80 kVp | 57-85 kVp | 60-84 kVp | | mA | 1-16 mA | 4-10 mA | 2-16 mA | 4-10mA | | Digital Sensor | Y | Y | Y | Y | | Image Pixel size | 66µm | 96 µm | 96 µm | 96 µm | | Exposure Time | 2-17s | 11-12s | 12s | 8-10s | | Image Profiles | Pan, TMJ,
Ortho | Pan | Pan, TMJ,
Ortho | Pan, TMJ,
Ortho | | Operator Exposure
Control | Deadman
Switch | Deadman
Switch | Deadman
Switch | Deadman
Switch | | User Interface | Color
Touch Screen | Keypad and
LED Display | Color
Touch Screen | Color
Touch Screen | | X-Ray tube focal spot | $0.5mm^2$ | $0.4mm^2$ | $0.5mm^2$ | $0.5mm^2$ | | Magnification | 1.2 | 1.25 | 1.3 | 1.2 | | Column | Telescoping | Telescoping | Fixed | Telescoping | | Construction | Aluminum
castings with
plastic and
metal covers | Aluminum
extrusions with
plastic covers | Aluminum
castings with
plastic and
metal covers | Aluminum
castings with
plastic and
metal covers | The predicate devices show a range of specifications. The Progeny Vantage is equivalent to at least one of the predicate devices for each of the specifications excepting exposure time. The shaded areas in the table above show the areas of congruence. Exposure time, by itself, is not a critical specification for comparison, as the equivalence in sensors across two of the predicate devices indicates a similar dose to achieve the same level of image detail. {3}------------------------------------------------ ### VI. Safety and Effectiveness Information Safety and effectiveness is demonstrated by: Performance testing and verification to meet product specifications. Software testing to validate software design and performance. Hazard analysis and risk level assessment. Same indications for use as predicate devices. All of the above steps and evaluations combine to demonstrate that the Panoramic Extraoral Radiographic Imaging System is safe and effective when the device is used as labeled. VII. Conclusion The Progeny Vantage Panoramic Extraoral Radiographic Imaging System is determined to be substantially equivalent to the predicate devices, the Planmeca Promax, the Instrumentarium Orthopantomograph OP100D, and the Gendex. The Panoramic Extraoral Radiographic Imaging System shares the same indications for use, materials, design, operational and functional features to the currently marketed predicate devices listed in section III of this summary. The Panoramic Extraoral Radiographic Imaging System is safe and effective when the device is used as labeled. {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized design featuring three curved shapes that resemble a person with outstretched arms. ## DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 # JUL 2009 Midmark % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313 Re: K091866 Trade/Device Name: Progeny Vantage Panoramic X-Ray System Regulation Number: 21 CFR 872.1800 Regulation Name: Extraoral source x-ray system Regulatory Class: II Product Code: MUH Dated: July 8, 2009 Received: July 9, 2009 ## Dear Mr. Job: 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 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. 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); medical device reporting of medical {5}------------------------------------------------ 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 the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/cdrl/mdr/ 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 (800) 638-2041 or (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Iveline M. Morris Janine M. Morris Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ ## Indications for Use 510(k) Number (if known): Ko91866 Progeny Vantage Panoramic X-Ray System Device Name: Indications For Use: The indications for use of the Progeny Vantage Extra-Oral Panoramic X-Ray System is to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. Prescription Use (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Division of Reproductive, Abdominal and Radiological Devices 510(k) Number K091866 Page 1 of 1 --- **Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/MUH/K091866](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/MUH/K091866) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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