(48 days)
Not Found
No
The device description focuses on mechanical components (balloon, tube, air supply unit) and their function in assisting endoscope positioning. There is no mention of data processing, algorithms, or learning capabilities.
No.
The device's intended use is to ensure positioning of a standard endoscope during endoscopy, not to provide direct therapeutic treatment.
No
The device is described as an accessory to an endoscope intended to ensure positioning and facilitate advancement of the endoscope, not for diagnostic purposes.
No
The device description clearly outlines physical components including a disposable balloon system, an Air Supply Unit (ASU), and a Single Balloon - Air Supply Unit (SB ASU), all of which are hardware.
Based on the provided information, the NaviAid™ BGC device is not an In Vitro Diagnostic (IVD).
Here's why:
- Intended Use: The intended use is to "ensure positioning of a standard endoscope during endoscopy of the small and large intestine." This describes a device used during a medical procedure to facilitate the physical manipulation and placement of another medical device (the endoscope).
- Device Description: The description details a mechanical system involving a balloon, inflation tube, and air supply unit used to anchor and guide the endoscope. It focuses on the physical interaction with the anatomy to aid in navigation.
- Lack of Diagnostic Function: There is no mention of the device being used to analyze samples (like blood, tissue, or other bodily fluids) or to provide information about a patient's health status or disease. IVDs are specifically designed for these purposes.
The NaviAid™ BGC device is a medical device used to assist in an endoscopic procedure, but it does not perform an in vitro diagnostic function.
N/A
Intended Use / Indications for Use
The NaviAid™ BGC device is an accessory to an endoscope and is intended to ensure positioning of a standard endoscope during endoscopy of the small and large intestine (standard endoscope-i.e., an endoscope that has an instrument channel that is at least 3.7mm diameter and is used for standard endoscopic visualization).
Product codes (comma separated list FDA assigned to the subject device)
ODC
Device Description
The modified NaviAid™ BGC is an on-demand disposable that is inserted through the instrument channel of the endoscope in order to enable advancement and positioning of a standard endoscope in the small and large intestine.
The modified NaviAid™ BGC system comprises a disposable balloon system and an Air Supply Unit ("ASU") or a Single Balloon - Air Supply Unit ("SB ASU") for inflating and deflating the balloon system.
The role of the BGC disposable is to facilitate advancement of a standard endoscope into the small and large intestine. The NaviAid™ BGC disposable includes the BGC Balloon and the BGC inflation tube. The balloon is inflated by ambient air. The ASU or SB ASU operate and control the inflation and deflation of the balloon through a foot-pedal. The balloon is connected to a dedicated inflation tube that runs inside the instrument channel of the endoscope, and is connected at its proximal (user) end to the ASU or SB ASU.
The BGC balloon can be advanced ahead of the endoscope tip or pulled back through pushing/pulling action on the BGC inflation tube at its proximal side, outside the patient's body. When the BGC balloon is advanced and then inflated, it functions as a distal anchor, to which the endoscope tip is advanced, and the BGC inflation tube serves as a rail that leads the endoscope as it is pushed towards the anchoring BGC balloon.
The balloon and tube negligibly compromise the endoscope's flexibility, or its field of view. Additionally, the BGC disposable negligibly compromise the maneuverability of the endoscope's tip and does not limit the usage of any standard endoscopy tools. During the procedure the disposable can be removed from the instrument channel of the endoscope and a therapy tool may be inserted instead.
The NaviAid™ BGC disposable is intended for single use, while the ASU and SB ASU are re-usable.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
small and large intestine
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)
Non-Clinical Performance Data:
Performance tests relating to the BGC Disposable component are located in the submission of the first predicate device, the NaviAid™ BGC device (document number K102616).
Performance tests relating to the SB ASU component are located in the submission of the second predicate device, the NaviAid™ ICVI device (document number K110291).
Clinical Performance Data: Not Applicable
Conclusions Drawn from Non-Clinical and Clinical Tests:
The non-clinical tests demonstrated that the modified NaviAid™ BGC device with the alternative SB ASU component meets its design and performance specifications. The modified NaviAid™ BGC device may be safely and effectively used in procedures in order to ensure the positioning of a standard endoscope in endoscopy of the small and large intestine and reach depths of the intestine that may not otherwise be accessible with a standard endoscope device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
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
§ 876.1500 Endoscope and accessories.
(a)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.(b)
Classification —(1)Class II (special controls). The device, when it is an endoscope disinfectant basin, which consists solely of a container that holds disinfectant and endoscopes and accessories; an endoscopic magnetic retriever intended for single use; sterile scissors for cystoscope intended for single use; a disposable, non-powered endoscopic grasping/cutting instrument intended for single use; a diagnostic incandescent light source; a fiberoptic photographic light source; a routine fiberoptic light source; an endoscopic sponge carrier; a xenon arc endoscope light source; an endoscope transformer; an LED light source; or a gastroenterology-urology endoscopic guidewire, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 876.9.(2) Class I for the photographic accessories for endoscope, miscellaneous bulb adapter for endoscope, binocular attachment for endoscope, eyepiece attachment for prescription lens, teaching attachment, inflation bulb, measuring device for panendoscope, photographic equipment for physiologic function monitor, special lens instrument for endoscope, smoke removal tube, rechargeable battery box, pocket battery box, bite block for endoscope, and cleaning brush for endoscope. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807of this chapter, subject to the limitations in § 876.9.
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Page 1 of 5
SECTION 7 - 510(K) SUMMARY OF SAFETY & EFFECTIVENESS
MODIFIED NAVIAID™ BGC DEVICE
AUG - 9 2011
510(k) Number K111760
Applicant's Name:
| Company name: | Smart Medical Systems Ltd. |
|---|---|
| Address: | 10 Hayetsira Str. |
| Ra'anana 43663 | |
| ISRAEL | |
| Tel.: | +972-9-7444321 |
| Fax: | +972-9-7444543 |
| e-mail: | ayoselzon@smartmedsys.com |
Contact Person:
| Official Correspondent: | Adva Yoselzon |
|---|---|
| Company name: | Smart Medical Systems Ltd. |
| Address: | 10 Hayetsira Str. |
| Ra'anana 43663 | |
| ISRAEL | |
| Tel.: | +972-9-7444321 |
| Fax: | +972-9-7444543 |
| e-mail: | ayoselzon@smartmedsys.com |
Name of the device:
NaviAid™ BGC device
Trade or proprietary name, if applicable:
NaviAid™ BGC device
Common or usual name:
NaviAid™ Balloon Guided Colonoscopy (NaviAid™ BGC Device)
Establishment Registration No.:
3005261802
1
K111760
page 2 of 5
Classification Name:
Endoscope and accessories
Classification:
FDA has classified Endoscope and accessories devices as a Class II medical device, with product code ODC and 21 CFR classification code 876.1500. Review by the Gastroenterology/Urology Devices Panel.
Predicate Device:
The modified NaviAid™ BGC device is substantially equivalent to the cleared NaviAid™ BGC device (manufactured by Smart Medical Systems Ltd. and the subject of 510(k) document no. K102616) and to the cleared NaviAid™ ICVI device (manufactured by Smart Medical Systems Ltd. and the subject of 510(k) document no. K110291), A comparison table and detailed discussion are presented in Section 10 of this application.
Device Description:
The modified NaviAid™ BGC is an on-demand disposable that is inserted through the instrument channel of the endoscope in order to enable advancement and positioning of a standard endoscope in the small and large intestine.
The modified NaviAid™ BGC system comprises a disposable balloon system and an Air Supply Unit ("ASU") or a Single Balloon - Air Supply Unit ("SB ASU") for inflating and deflating the balloon system.
The role of the BGC disposable is to facilitate advancement of a standard endoscope into the small and large intestine. The NaviAid™ BGC disposable includes the BGC Balloon and the BGC inflation tube. The balloon is inflated by ambient air. The ASU or SB ASU operate and control the inflation and deflation of the balloon through a foot-pedal. The balloon is connected to a dedicated inflation tube that runs inside the instrument channel of the endoscope, and is connected at its proximal (user) end to the ASU or SB ASU.
The BGC balloon can be advanced ahead of the endoscope tip or pulled back through pushing/pulling action on the BGC inflation tube at its proximal side, outside the patient's body. When the BGC balloon is advanced and then inflated, it functions as a distal anchor, to which the endoscope tip is advanced, and the BGC inflation tube serves as a rail that leads the endoscope as it is pushed towards the anchoring BGC balloon.
7-2
2
K /// 760
Page 3 of 5
The balloon and tube negligibly compromise the endoscope's flexibility, or its field of view. Additionally, the BGC disposable negligibly compromise the maneuverability of the endoscope's tip and does not limit the usage of any standard endoscopy tools. During the procedure the disposable can be removed from the instrument channel of the endoscope and a therapy tool may be inserted instead.
The NaviAid™ BGC disposable is intended for single use, while the ASU and SB ASU are re-usable.
Intended Use / Indication for Use:
The NaviAid™ BGC device is an accessory to an endoscope and is intended to ensure positioning of a standard endoscope during endoscopy of the small and large intestine (standard endoscope-i.e., an endoscope that has an instrument channel that is at least 3.7mm diameter and is used for standard endoscopic visualization).
Comparison of Technological Characteristics with the predicate device:
Modification to the NaviAid™ BGC device includes only the addition of the SB ASU as an alternative component to the ASU.
The SB ASU component of the modified NaviAid™ BGC device is identical to the SB ASU component of the cleared NaviAid™ ICVI Device (K110291) and their technological characteristic are the identical. The BGC Disposable was not changed or altered and therefore the modified NaviAid™ BGC disposable is also identical to the cleared NaviAid™ BGC disposable (K102616).
Non-Clinical Performance Data
Performance tests relating to the BGC Disposable component are located in the submission of the first predicate device, the NaviAid™ BGC device (document number K102616).
Performance tests relating to the SB ASU component are located in the submission of the second predicate device, the NaviAid™ ICVI device (document number K110291).
3
K111 760
page 4 of 5
Clinical Performance Data
Not Applicable
Conclusions Drawn from Non-Clinical and Clinical Tests:
The non-clinical tests demonstrated that the modified NaviAid™ BGC device with the alternative SB ASU component meets its design and performance specifications. The modified NaviAid™ BGC device may be safely and effectively used in procedures in order to ensure the positioning of a standard endoscope in endoscopy of the small and large intestine and reach depths of the intestine that may not otherwise be accessible with a standard endoscope device.
Substantial Equivalence:
In summary, the modified NaviAid™ BGC device is substantially equivalent to the cleared NaviAid™ BGC device. The only difference is the addition of the SB ASU as an alternative to the ASU. The intended use, basic technology, principle of operation, specifications and safety requirements of the modified NaviAid™ BGC device and the cleared NaviAid™ BGC are the similar.
The modified NaviAid™ BGC is also substantially equivalent to the cleared NaviAid™ ICVI device. The SB ASU component of the modified NaviAid™ BGC device is identical to the SB ASU component of the cleared NaviAid™ ICVI device. The intended use, basic technology, principle of operation, specifications and safety requirements of the SB ASU are identical.
Consequently, the modified NaviAid™ BGC device is substantially equivalent to the cleared NaviAid™ BGC device and to the cleared NaviAid™ ICVI device. The minor differences do not raise any new questions of safety and effectiveness.
Performance Standards:
-
- Electrical & Mechanical Safety Testing (IEC 60601-1)
-
Electromagnetic Compatibility Testing (IEC 60601-1-2)
-
Software Validation (IEC 60601-1-4 & FDA Guidelines)
Results of the above mentioned performance testing (including Electrical & Mechanical Safety, Electromagnetic Compatibility and software validation) are
4
K 11176.0
page 5 of 5
provided in 510(k) number K110291 of the cleared NaviAid™ ICVI device. Nevertheless, for convenience, the completed Standards Data Form (FDA Form #3654) for these standards is provided in Appendix 11-5 of this submission.
5
Image /page/5/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle or bird-like symbol with three curved lines representing its body and wings. The bird is positioned within a circle, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged around the circumference of the circle.
Food and Drug Administration 10903 New Hampshire Avenue Document Mail Center - WO66-G609 Silver Spring. MD 20993-0002
Mrs. Adva Yoselzon QA Manager and Director of Clinical & Regulatory Affairs Smart Medical Systems Ltd. 10 Hayeisira Str. RA'ANANA 43663 ISRAEI.
Re: K111760
Trade/Device Name: NaviAidTM BGC Device Regulation Number: 21 CFR$ 876.1500 Regulation Name: Endoscope and accessories Regulatory Class: II Product Code: ODC Dated: July 28, 2011 Received: August 2, 2011
AUG - 9 2011
Dear Mrs. Yoselzon:
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 10 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.
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 device-related
6
Page 2
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/MedicalDevices/Safety/ReportaProblem/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 (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
Hubert Lehman MD
Herbert P. Lerner, M.D., Director (Acting) Division of Reproductive, Gastro-Renal and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
7
K/// 76.0
SECTION 6 INDICATIONS FOR USE STATEMENT
11/760 510(k) Number (if known): Y
Device Name:
NaviAid™ BGC Device
Indications for use:
The NaviAid™ BGC device is an accessory to an endoscope and is intended to ensure positioning of a standard endoscope during endoscopy of the small and large intestine (standard endoscope-i.e., an endoscope that has an instrument channel that is at least 3.7mm diameter and is used for standard endoscopic visualization).
Prescription Use Use (Per 21 C.F.R. 801 Subpart D)
OR
Over-The-Counter
(Optional Format Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
hozu K Wh
ve. Gastro-Rena
6-1