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FDA Presentation P010035 Computerized Thermal Imaging, Inc. CTI™ BCS 2100.

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Presentation on theme: "FDA Presentation P010035 Computerized Thermal Imaging, Inc. CTI™ BCS 2100."— Presentation transcript:

1 FDA Presentation P010035 Computerized Thermal Imaging, Inc. CTI™ BCS 2100

2 Modular PMA Submission M990018 Module 1 – Preliminary Information Review John Monahan Module 2 – Software Review Joseph Jorgens III Module 3 - Manufacturing Review Xuan Vo Module 4 – Engineering Review Jim Seiler

3 P010035 Reviewers Lead Reviewer – John C. Monahan Clinical Reviewer – Wm. Sacks, Ph.D., M.D. Statistical Reviewer – Harry Bushar, Ph.D. Bioresearch Monitor – Kevin Hopson

4 Proposed Indication for Use The CTI BCS2100 is intended “for use as an adjunct to mammography to safely avoid biopsy of benign breast masses that would otherwise have undergone biopsy. A physician should not base a decision for patient care solely on the results of testing with this device...other findings and risk factors associated with a specific patient.

5 Proposed Indication for Use (cont.) “The CTI BCS2100 provides additional information to guide a breast biopsy recommendation. …use of the CTI BCS2100 should be limited to the evaluation of breast lesions that include ’mass’ as a lesion descriptor....

6 Proposed Indication for Use (cont.) “It is recommended that...all patients receiving a negative IR test result be similar to the recommendation for care of a mass that is assigned to mammographic category 3.That is, a short interval follow-up is recommended in order to establish the stability of the finding.”


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