The LungPoint Tools are endoscopic tools intended to be used with LungPoint Software guided bronchoscopes. The LungPoint Sheath is intended to be used as a working channel through which endoscopic tools may be introduced to targeted tissue. The LungPoint Dilation Balloon is intended to dilate tissue of the bronchial tree and may be inserted through the LungPoint Sheath or directly through the working channel of the bronchoscope. Not for pediatric use.

Device Description

The LungPoint Tools are endoscopic tools used during bronchoscopy procedures. The LungPoint Sheath is designed to be used with a bronchoscope to provide a working channel through which endoscopic tools, such as needles, dilation balloons, or other endoscopic devices may be introduced to the targeted lung tissue within the respiratory organs. The LungPoint Dilation Balloon is used to dilate tissue of the bronchial tree and may be inserted through the sheath or directly through the working channel of the bronchoscope. The bronchoscope is advanced to a predefined target following guidance of the LungPoint Software (previously cleared under 510(k) #K 12051 to guide endoscopic tools or catheters in the lungs or to enable marker placement in soft lung tissue).

The materials used in the LungPoint Tools are commonly used medical grade materials and include platinum iridium markers.

AI/ML Overview

This document describes the validation of the LungPoint™ Tools (LungPoint Sheath and LungPoint Dilation Balloon). It's important to note that this is a 510(k) summary for a medical device (tools), not an AI/ML device, so many of the requested fields related to AI/ML device validation (e.g., effect size with AI assistance, training set details) are not applicable (N/A). The summary focuses on demonstrating substantial equivalence to predicate devices through physical and functional performance testing.

Acceptance Criteria and Device Performance

The acceptance criteria for the LungPoint Tools were based on meeting pre-determined specifications for functional and performance tests. The specific numerical acceptance criteria are not detailed in the provided text but are stated to have been met.

Acceptance Criteria Category	Reported Device Performance
Dimensional testing	Met pre-determined criteria
Joint/tensile test	Met pre-determined criteria
Simulated use	Met pre-determined criteria
Balloon fatigue/burst pressure	Met pre-determined criteria (e.g., LungPoint Dilation Balloon rated burst pressure 20 atm)
Balloon deflation time	Met pre-determined criteria
Radiopacity	Met pre-determined criteria

Study Details

Sample size used for the test set and the data provenance:
- Test set sample size: Not explicitly stated in terms of number of devices tested, but the performance data refers to a series of physical and functional tests performed on the devices themselves.
- Data provenance: The tests were conducted internally by the manufacturer (Broncus Medical, Inc.) to verify the design and safety of the devices. The context suggests these were laboratory-based engineering and performance tests relevant to the physical characteristics and function of the tools.
Number of experts used to establish the ground truth for the test set and the qualifications of those experts:
- N/A. This device is a physical medical tool, and its "ground truth" is established by its physical specifications and functional performance under laboratory conditions, not by expert interpretation of data or images. Performance was verified against pre-determined engineering and safety specifications.
Adjudication method (e.g., 2+1, 3+1, none) for the test set:
- N/A. Adjudication methods are typically relevant for interpretive tasks involving human experts, which is not the case for this type of device performance testing.
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:
- N/A. This is not an AI/ML device.
If a standalone (i.e. algorithm only without human-in-the-loop performance) was done:
- N/A. This is not an AI/ML device.
The type of ground truth used (expert consensus, pathology, outcomes data, etc.):
- The "ground truth" for these physical tools is their engineering specifications, material properties, and functional performance benchmarks as established during the design and manufacturing process. The goal was to demonstrate that the devices met these pre-determined acceptance criteria and performed comparably to predicate devices.
The sample size for the training set:
- N/A. This is not an AI/ML device.
How the ground truth for the training set was established:
- N/A. This is not an AI/ML device.

Summary

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131234

510(k) Summary

Date of Summary

October 10, 2013

2. 510(k) Applicant

Broncus Medical, Inc. 1400 N. Shoreline Blvd, Suite A8 Mountain View, California 94043 (650) 428-1600 Phone: FAX: (650) 428-1542

OCT 15 2013

Contact Person:	Gary Kaplan
Phone:	(650) 428-1600
Fax:	(650) 428-1542
e-mail:	gkaplan@broncus.com

3. Device Overview

Trade Name:	LungPoint™ Tools (LungPoint Sheath and LungPoint Dilation Balloon)
Common Name:	Sheath and Dilation Balloon
Classification Name:	Bronchoscope and Accessories21 CFR 874.4680Product Code EOQ

4. Predicate Device

The predicate devices identified are as follows:

Trade Name	510(k) Submitter	510(k) Number
CRE Pulmonary BalloonDilatation Catheter	Boston ScientificCorporation	K023337, cleared to market onNovember 18, 2002
Olympus Guide Sheath	Olympus MedicalSystems Corporation	K060243, cleared to market onJune 23, 2006

5. Device Description

The LungPoint Tools are endoscopic tools used during bronchoscopy procedures. The LungPoint Sheath is designed to be used with a bronchoscope to provide a working

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channel through which endoscopic tools, such as needles, dilation balloons, or other endoscopic devices may be introduced to the targeted lung tissue within the respiratory organs. The LungPoint Dilation Balloon is used to dilate tissue of the bronchial tree and may be inserted through the sheath or directly through the working channel of the bronchoscope. The bronchoscope is advanced to a predefined target following guidance of the LungPoint Software (previously cleared under 510(k) #K 12051 to guide endoscopic tools or catheters in the lungs or to enable marker placement in soft lung tissue).

The materials used in the LungPoint Tools are commonly used medical grade materials and include platinum iridium markers.

CatalogNumber	Working Length	MaximumCatheter OuterDiameter (OD)	Catheter InternalDiameter (ID)	Minimum accessorylength for use throughsheath
10007-1	900mm	2.65mm	2.0mm	965mm

The LungPoint Sheath has the following specifications:

The LungPoint Dilation Balloon has the following specifications:

CatalogNumber	Balloon Size(OD x length)	Rated BalloonPressure	MaximumCatheter OuterDiameter (OD)	CatheterLength/working length
10008-1	4mm x 6mm	20atm	1mm	1430mm/975mm

6. Intended Use

7. Comparison to Predicate Device

The LungPoint Tools are commonly used endoscopic tools with the same technological characteristics as the predicate devices. The indications for use of the LungPoint Tools for use with a bronchoscope guided by the LungPoint Software are all within the intended use of the predicate devices, which is to aid in reaching a target in the respiratory organ

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either directly as is the case with the sheath or through dilating target tissue with the dilation balloon. The technological characteristics of the subject devices are the same as those of the predicate devices with the following exceptions

LungPoint Balloon: balloon size and length, balloon burst pressure and balloon . catheter length as outlined.

	CRE Pulmonary BalloonDilatation Catheter(K023337)	LungPoint DilationBalloon
Balloon Size and Inflation(balloon pressure)	8mm @ 3 ATM9mm @ 5.5 ATM10mm @ 9 ATM	4mm @ 10 ATM
Catheter Length (cm)	155	143
Balloon Length (cm)	3.0	0.6
Rated Burst Pressure (atmospheres)	9	20

LungPoint Sheath: stylet, catheter ID/OD and catheter length as outlined. .

	Olympus Guide Sheath(K060243)	LungPoint Sheath
Stylet Provided	No	Yes - used to enhancepushability and to preventairway mucosa enteringsheath
Catheter ID/OD	2.1/2.7 mm	2.0/2.6 mm
Catheter Length	900 mm	975 mm

None of these differences raise new questions of safety and effectiveness. Performance of the subject devices has been verified by use of accepted methods.

8. Performance Data

The design and safety of the LungPoint Tools were verified by performing functional and performance testing. All tests were designed to subject the sheath and dilation balloon to stresses that exceed those which would be encountered during clinical use. Testing included the following:

Dimensional testing -
Joint/tensile test
Simulated use -
Balloon fatigue/burst pressure -
Balloon deflation time -
Radiopacity. -

All testing results met the pre-determined acceptance criteria that were established in the test protocols. Based on the testing the LungPoint Tools are as safe, as effective, and perform at least as safely and effectively as the predicate devices.

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9. Safety and Effectiveness

The LungPoint Tools labeling contains instructions for use and any necessary cautions and warnings, to provide for safe and effective use of the devices. The biocompatibility assessment of all patient contacting materials was performed in accordance with ISO 10993. Biological Evaluation of Medical Devices. Specifically, cytotoxicity, sensitization, intracutaneous reactivity and systemic toxicity (acute) were tested. In addition, the devices are sterilized using e-beam sterilization.

10. Conclusion

Based on the testing the LungPoint Tools are as safe, as effective, and perform at least as safely and effectively as the predicate devices.

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Image /page/4/Picture/1 description: The image shows the logo for the Department of Health & Human Services (HHS) in the United States. The logo consists of a stylized graphic element resembling an abstract human form or a bird in flight. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" is arranged in a circular fashion around the graphic.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-002

October 15, 2013

Broncus Medical, Inc. c/o Mr. Mark Job Regulatory Technology Services, LLC 1394 25th Street, NW Buffalo, MN 55313

Re: K131234

Trade/Device Name: LungPoint™ Tools (LungPoint Sheath and LungPoint Dilation Balloon) Regulation Number: 21 CFR 874.4680 Regulation Name: Bronchoscope (Flexible or Rigid) and Accessories Regulatory Class: Class II Product Code: EOQ Dated: August 26, 2013 Received: August 27, 2013

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. 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. Mark Job

""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 (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 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.

Eric A.Männ -S

for Malvina B. Eydelman, M.D. Director Division of Ophthalmic and Ear, Nose and Throat Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications for Use

510(k) Number (if known): K131234

Device Name:

LungPoint Tools - LungPoint Dilation Balloon and LungPoint Sheath

The LungPoint Tools are endoscopic tools intended to be Indications for Use: used with LungPoint Software guided bronchoscopes. The LungPoint Sheath is intended to be used as a working channel through which endoscopic tools may be introduced to targeted tissue. The LungPoint Dilation Balloon is intended to dilate tissue of the bronchial tree and may be inserted through the LungPoint Sheath or directly through the working channel of the bronchoscope. Not for pediatric use.

× 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)

Page __ of ___________________________________________________________________________________________________________________________________________________________________

Srinivaš

Regulation Number and Section

§ 874.4680 Bronchoscope (flexible or rigid) and accessories.

(a)
Identification. A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. It is typically used with a fiberoptic light source and carrier to provide illumination. The device is made of materials such as stainless steel or flexible plastic. This generic type of device includes the rigid ventilating bronchoscope, rigid nonventilating bronchoscope, nonrigid bronchoscope, laryngeal-bronchial telescope, flexible foreign body claw, bronchoscope tubing, flexible biopsy forceps, rigid biopsy curette, flexible biopsy brush, rigid biopsy forceps, flexible biopsy curette, and rigid bronchoscope aspirating tube, but excludes the fiberoptic light source and carrier.(b)
Classification. Class II.