Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit

K203296 · Gold Standard Diagnostics · LSR · Mar 22, 2021 · Microbiology

Device Facts

• Record ID: K203296
• Device Name: Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit
• Applicant: Gold Standard Diagnostics
• Product Code: LSR · Microbiology
• Decision Date: Mar 22, 2021
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 866.3830
• Device Class: Class 2

Indications for Use

The Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is intended as a qualitative test for the detection of IgG antibodies to B. burgdorferi sensu stricto in human serum from symptomatic patients or people suspected of infection. When used as the first-tier screening test, positive and equivocal results must be supplemented through additional testing by one of the following methods: · Standard two-tier test methodology (STTT) using an IgG blot test following current interpretation guidelines, OR • Modified two-tier test methodology (MTTT) using the Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test. The assay can also be used as a second-tier confirmation test using the MTTT methodology when used with the Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test as the first-tier screening test. Positive test results by either the STTT or MTTT methodology are supportive evidence for the presence of antibodies and exposure to Borrelia burgdorferi, the cause of Lyme disease. A diagnosis of Lyme disease should be made based on the presence of Borrelia burgdorferi antibodies, history, symptoms, and other laboratory findings.

Device Story

ELISA test kit detects IgG antibodies to B. burgdorferi in human serum; utilizes antigen-coated microtiter plates (B. burgdorferi B31/2591 lysates and recombinant VlsE). Procedure involves sample incubation, washing, addition of HRP-conjugated goat anti-human IgG, and chromogenic TMB substrate. Enzymatic reaction produces color change (blue to yellow after stop solution); measured photometrically at 450 nm. Used in clinical laboratories by trained personnel. Results support Lyme disease diagnosis when combined with clinical history and symptoms. Supports both Standard Two-Tier Testing (STTT) and Modified Two-Tier Testing (MTTT) algorithms. MTTT utilizes a second ELISA as a confirmatory step, potentially improving sensitivity in early and disseminated disease stages compared to traditional Western blot confirmation.

Clinical Evidence

Clinical sensitivity evaluated on 125 characterized samples (early, disseminated, late Lyme) and 280 CDC reference panel samples. In sensitivity study, MTTT algorithm showed higher agreement with clinical diagnosis (Early: 48.4% vs 8.1%; Disseminated: 81.8% vs 22.7%) compared to STTT. CDC panel results confirmed improved sensitivity in early Lyme (60.0% vs 33.3%) and neurological Lyme (85.7% vs 14.3%). Negative percent agreement with STTT was 96.7% (95% CI: 94.7-98.2%).

Technological Characteristics

ELISA-based immunoassay; 96-well microplate format. Antigens: B. burgdorferi B31/2591 lysates and recombinant VlsE protein. Detection: Photometric measurement at 450 nm using TMB substrate. Reagents: Conjugate (HRP-labeled goat anti-human IgG), wash buffer, stop solution. Standalone diagnostic test; no specialized software or connectivity required beyond standard microplate reader.

Indications for Use

Indicated for qualitative detection of IgG antibodies to B. burgdorferi sensu stricto in human serum from symptomatic patients or those suspected of Lyme disease infection.

Regulatory Classification

Identification

Treponema pallidum treponemal test reagents are devices that consist of the antigens, antisera and all control reagents (standardized reagents with which test results are compared) which are derived from treponemal sources and that are used in the fluorescent treponemal antibody absorption test (FTA-ABS), the Treponema pallidum immobilization test (T.P.I.), and other treponemal tests used to identify antibodies to Treponema pallidum directly from infecting treponemal organisms in serum. The identification aids in the diagnosis of syphilis caused by bacteria belonging to the genus Treponema and provides epidemiological information on syphilis.

Predicate Devices

• Trinity Biotech MarDx Borrelia burgdorferi EIA IgG Test Kit (K894224)
• Gold Standard Diagnostics Borrelia burgdorferi IgG Blot Test Kit (K113847)

Submission Summary (Full Text)

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FDA U.S. FOOD & DRUG ADMINISTRATION

# 510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY

ASSAY ONLY

## I Background Information:

A 510(k) Number

K203296

B Applicant

Gold Standard Diagnostics

C Proprietary and Established Names

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit

D Regulatory Information

| Product Code(s) | Classification | Regulation Section | Panel |
| --- | --- | --- | --- |
| LSR | Class II | 21 CFR 866.3830 - Treponema Pallidum
Treponemal Test Reagents | MI - Microbiology |

## II Submission/Device Overview:

### A Purpose for Submission:

To obtain a substantial equivalence determination and FDA clearance for a new device and to obtain a substantial equivalence determination and FDA clearance for a modified intended use for a previously cleared medical device. This regulatory filing follows the FDA guidance document titled “Bundling Multiple Devices or Multiple Indications in a Single Submission”1. For these devices, bundling is appropriate since the device review presented scientific and regulatory issues that were most efficiently addressed during a single review. In determining whether a bundled submission was appropriate FDA considered that: (i) the supporting data are similar; (ii) primarily one review division/group will be involved; and (iii) the devices or indications for use are similar.

### B Measurand:

Food and Drug Administration
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002
www.fda.gov

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Anti-Borrelia burgdorferi antibodies

## C Type of Test:

Enzyme-linked immunosorbent assay (ELISA)

## III Intended Use/Indications for Use:

### A Intended Use(s):

See Indications for Use below.

### B Indication(s) for Use:

**Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit**

The Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is intended as a qualitative test for the detection of IgG antibodies to B. burgdorferi sensu stricto in human serum from symptomatic patients or people suspected of infection. When used as the first-tier screening test, positive and equivocal results must be supplemented through additional testing by one of the following methods:

a) Standard two-tier test methodology (STTT) using an IgG blot test following current interpretation guidelines, OR

b) Modified two-tier test methodology (MTTT) using the Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test.

The assay can also be used as a second-tier confirmation test using the MTTT methodology when used with the Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test as the first-tier screening test.

Positive test results by either the STTT or MTTT methodology are supportive evidence for the presence of antibodies and exposure to Borrelia burgdorferi, the cause of Lyme disease. A diagnosis of Lyme disease should be made based on the presence of Borrelia burgdorferi antibodies, history, symptoms, and other laboratory findings.

**Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit**

The Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit is intended as a qualitative test for the detection of IgG and IgM class antibodies to VlsE and OspC antigens from Borrelia burgdorferi sensu stricto in human serum from symptomatic patients or people suspected of having Lyme disease. When used as the first-tier screening test, positive and equivocal results must be confirmed through additional testing by one of the following methods:

a) Standard two-tier test methodology (STTT) using an IgG and/or IgM blot testing following current interpretation guidelines, OR

b) Modified two-tier test methodology (MTTT) using one or more of the following three ELISA based assays: Gold Standard Diagnostics Borrelia burgdorferi IgG/IgM ELISA Test, Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test, Gold Standard Diagnostics Borrelia burgdorferi IgM ELISA Test.

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The assay can also be used as a second-tier confirmation test using the MTTT methodology when used with one or more of the following three ELISA based assays: Gold Standard Diagnostics Borrelia burgdorferi IgG/IgM ELISA Test, Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test, Gold Standard Diagnostics Borrelia burgdorferi IgM ELISA Test.

Positive test results by either the STTT or MTTT methodology are supportive evidence for the presence of antibodies and exposure to Borrelia burgdorferi, the cause of Lyme disease. A diagnosis of Lyme disease should be made based on the presence of Borrelia burgdorferi antibodies, history, symptoms, and other laboratory findings.

## C Special Conditions for Use Statement(s):

Rx - For Prescription Use Only

## D Special Instrument Requirements:

None

## IV Device/System Characteristics:

### A Device Description:

The kit includes 12 x 8 well Antigen Coated strips, Conjugate, Substrate, Stop Solution, Wash Buffer, Diluent, Negative Control, Positive Control, and Cutoff Control. The controls are provided to determine if the assay is functioning properly and to determine the antibody level. The reagents are sufficient for 96 determinations.

During the test procedure, antibodies to B. burgdorferi (sensu stricto) if present in the human serum sample will bind to the antigens coated onto the wells forming antigen-antibody complexes. Excess antibodies are removed by washing. A conjugate of goat anti-human IgG antibodies conjugated with horseradish peroxidase is then added, which binds to the antigen-antibody complexes. Excess conjugate is removed by washing. This is followed by the addition of a chromogenic substrate, tetramethylbenzidine (TMB). If specific antibodies to the antigen are present in the patients' serum, a blue color will develop. The enzymatic reaction is then stopped with a stopping solution causing the contents of the well to turn yellow. The wells are read photometrically with a microplate reader at 450 nm.

The antigens used in the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test kit is a combination of B. burgdorferi sensu stricto strain B31 lysate, B. burgdorferi sensu stricto strain 2591 lysate, and a recombinant VlsE from B. burgdorferi sensu stricto strain B31. The lysates use spirochetes growing in BSK-H complete medium until mid-exponential phase. The recombinant VlsE protein is produced in E. coli SURE2 cells and purified by affinity chromatography. The purity of each antigen is assayed by SDS-PAGE followed by Coomassie staining and/or Western blotting.

### V Substantial Equivalence Information:

### A Predicate Device Name(s):

Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit, Borrelia burgdorferi Igg Blot Test

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B Predicate 510(k) Number(s):

K200025, K113847

C Comparison with Predicate(s):

| Device & Predicate Device(s): | K203296 | K200025 | K113847 |
| --- | --- | --- | --- |
| Device Trade Name | Device 1: Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit
Device 2: Gold Standard Diagnostics Borrelia burgdorferi VlsE-OspC IgG/IgM ELISA Test Kit | Gold Standard Diagnostics Borrelia burgdorferi IgG Elisa Test Kit | Gold Standard Diagnostics Borrelia burgdorferi IgG Line Blot Test Kit |
| General Device Characteristic Similarities | | | |
| Intended Use/Indications For Use | These are two ELISA assays for the qualitative detection of B. burgdorferi antibodies in human serum. For a complete description of the Intended Use please see Item III B. above. | The Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit is intended as a qualitative presumptive (first-step) test for the detection of IgG antibodies to B. burgdorferi sensu stricto in human serum from symptomatic patients or people suspected of infection.
Positive and equivocal results must be supplemented by testing with a second-step Western blot assay. | The Gold Standard Diagnostics Borrelia burgdorferi B31 IgG Line Blot Test Kit is intended for the qualitative detection of IgG antibodies to B. burgdorferi sensu stricto (B31) in human serum. This test is intended for use in testing human serum samples which have been found positive or equivocal using an ELISA or IFA test procedure to provide supportive evidence of infection with B. burgdorferi. |
| Sample Matrix | Same | Human serum | Same |
| Controls Provided | Same | Positive, Cutoff, Negative | Same |
| Sample Processing | Same | Dilute Samples 1:100 | Same |

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| Assay Type | Same | Qualitative | Same |
| --- | --- | --- | --- |
| General Device Characteristic Differences | | | |
| Antigens | B. burgdorferi B31 strain,
B. burgdorferi 2591 strain,
B. burgdorferi recombinant VlsE B31 strain
Recombinant VlsE and OspC from B. burgdorferi strain B31 | B. burgdorferi B31 strain, B. burgdorferi 2591 strain, B. burgdorferi recombinant VlsE protein from B31 strain | B. burgdorferi B31 strain |
| Assay Format | Same | Antigen coated microtiter plate – 96 wells | Nitrocellulose strips |
| Technology | Same | ELISA | Immunoblot |
| Reagents Provided | Same | Diluent, Wash, Conjugate, Substrate, Stop Solution | Diluent/Wash, Conjugate, Substrate, |
| Volumes | Same | 100 μL sample, 50 μL substrate, 50 μL stop solution | 1500 μL sample, 1500 μL substrate, |
| Incubation | Same | 15/15/15 minutes at room temperature | 30/30/10-13 minutes at room temperature |
| Interpretation | Same | Optical density readings from spectrophotometer | Visual |
| Results Interpretation | Same | Convert to units.
Negative <9
Equivocal 9.0-11.0
Positive>11.0 | Compare to cutoff band |
| Reported Results | Same | Positive, Equivocal, Negative | Positive, Negative |

VI Standards/Guidance Documents Referenced:

None.

VII Performance Characteristics (if/when applicable):

A Analytical Performance:

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Note: This clearance is for a modified use for a previously cleared IVD, the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test Kit (K200025). Representative analytical study data are presented below.

1. Precision/Reproducibility:

To determine the precision of the Borrelia burgdorferi IgG ELISA Test, a within-lab precision study was conducted. A precision panel consisting of a negative sample, a high negative sample, a low positive sample, and a moderate positive sample, along with the kit controls, was tested in-house. The sample panel was masked and randomized. Each of the panel members was tested in duplicate, twice per day, for 12 days. The results are summarized in the following table:

Table 1. Precision Study Results

| Sample | N | Mean Units | | Within-Run | Between-Run | Between-Day | Total |
| --- | --- | --- | --- | --- | --- | --- | --- |
| Moderate Positive | 48 | 20.3 | SD | 1.488 | 1.312 | 1.257 | 1.439 |
| | | | CV | 7.3% | 6.5% | 6.2% | 7.1% |
| Low Positive | 48 | 11.5 | SD | 0.845 | 0.718 | 0.718 | 0.816 |
| | | | CV | 7.4% | 6.2% | 6.2% | 7.1% |
| High Negative | 48 | 8.3 | SD | 0.880 | 0.646 | 0.615 | 0.857 |
| | | | CV | 10.6% | 7.8% | 7.4% | 10.4% |
| Negative | 48 | 0.8 | SD | 0.116 | 0.049 | 0.076 | 0.113 |
| | | | CV | 14.2% | 6.5% | 10.0% | 14.8% |
| Positive Control | 48 | 17.2 | SD | 0.947 | 0.649 | 0.739 | 0.932 |
| | | | CV | 5.5% | 3.8% | 4.3% | 5.4% |
| Cutoff Control | 48 | 10.1 | SD | 0.241 | 0.115 | 0.285 | 0.264 |
| | | | CV | 2.7% | 1.1% | 2.8% | 2.6% |
| Negative Control | 48 | 0.4 | SD | 0.052 | 0.424 | 0.144 | 0.051 |
| | | | CV | 12.9% | 10.6% | 11.0% | 12.7% |

Reproducibility: A reproducibility panel consisting of a negative sample, a high negative sample, a low positive sample, and a moderate positive sample, along with the kit controls, was tested at three different sites. The sample panel was masked and randomized. Each of the panel members was tested in triplicate, twice per day, for five days. The Within-Run, Between-Run, Between-Days, and Between-Sites Standard Deviation and Coefficients of Variation (CV) were calculated. The sample panel was masked and randomized. The results are summarized in the following table:

Table 2. Reproducibility Study Results

| Sample | N | Mean Units | | Within-Run | Between-Run | Between-Day | Between-Sites | Total |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Moderate Positive | 90 | 21.0 | SD | 1.54 | 0.40 | 1.07 | 0.91 | 1.29 |
| | | | CV | 7.3% | 1.9% | 5.1% | 4.3% | 6.1% |
| Low Positive | 90 | 13.7 | SD | 0.72 | 0.34 | 1.09 | 1.24 | 1.28 |
| | | | CV | 5.5% | 2.6% | 8.0% | 9.1% | 9.3% |

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| High Negative | 90 | 6.6 | SD | 0.76 | 0.27 | 0.46 | 0.68 | 0.67 |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | CV | 11.7% | 4.1% | 7.0% | 10.3% | 10.2% |
| Negative | 90 | 3.0 | SD | 0.33 | 0.56 | 0.49 | 0.56 | 0.55 |
| | | | CV | 21.1% | 18.7% | 16.4% | 18.8% | 18.3% |
| Positive Control | 30 | 19.1 | SD | 0.65 | 0.67 | 0.67 | 0.63 | 0.62 |
| | | | CV | 3.5% | 3.5% | 3.5% | 3.3% | 3.2% |
| Cutoff Control | 60 | 10.0 | SD | 0.25 | 0.22 | 0.23 | 0.22 | 0.22 |
| | | | CV | 2.4% | 2.2% | 2.3% | 2.2% | 2.2% |
| Negative Control | 30 | 0.5 | SD | 0.08 | 0.06 | 0.06 | 0.50 | 0.50 |
| | | | CV | 11.0% | 11.0% | 11.0% | 9.5% | 9.6% |

2. Linearity:

Not Applicable.

3. Analytical Specificity/Interference:

Analytical Specificity: The analytical specificity was determined by testing 208 asymptomatic individuals' samples from endemic and non-endemic regions. The Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test results are summarized in the following table:

Table 3. Analytical Specificity Study Results

| | Number of samples | Number Positive/Equivocal | Analytical Specificity |
| --- | --- | --- | --- |
| Endemic Region | 103 | 4 | 96.1% |
| Non-endemic Region | 105 | 0 | 100% |

Cross-reactivity: A study using 377 samples was conducted to evaluate potential cross reactivity from different infections and disease conditions. The samples were obtained from serum vendors who confirmed their positivity for each respective marker or clinical diagnosis. The samples were tested on the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test. The results are summarized in the following table:

Table 4. Cross-reactivity Study Results

| Organism/Disease State | Samples Tested (N) | # Positive / (%) |
| --- | --- | --- |
| Tick borne Relapsing Fever IgG | 21 | 0 / 0% |
| Treponemal Infections | 23 | 0 / 0% |
| Rickettsia IgG | 25 | 6 / 24% |
| Ehrlichiosis IgG | 10 | 2 / 20% |
| Babesiosis IgG | 12 | 0 / 0% |
| Leptospirosis IgG | 10 | 8 / 80% |
| Parvovirus B19 IgG | 12 | 0 / 0% |
| Influenza A & B IgG | 12 | 0 / 0% |
| Epstein-Barr Virus IgM | 34 | 1 / 3% |

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| Herpes Simplex Virus IgG | 21 | 0 / 0% |
| --- | --- | --- |
| Varicella Zoster Virus | 16 | 1 / 6% |
| H. pylori IgM | 11 | 0 / 0% |
| Fibromyalgia | 32 | 0 / 0% |
| Rheumatoid Arthritis | 12 | 0 / 0% |
| Autoimmune Disease | 59 | 0 / 0% |
| Multiple Sclerosis | 23 | 0 / 0% |
| Severe Periodontitis | 23 | 0 / 0% |

Interfering Substances: The effect of potential interfering substances on samples using the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test was evaluated. Three samples, a high negative, an equivocal and a low positive were spiked with high levels of interferants and were tested along with serum without spiked interferants. The recommended concentrations from the guideline "Interference Testing in Clinical Chemistry" EP07-A3 from the Clinical and Laboratory Standards Institute were used (see table below). The tested substances did not affect the performance of the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test.

Table 5. Interference Testing Results

| Substance | Concentration | Interference |
| --- | --- | --- |
| Albumin | 60 mg/mL | None Detected |
| Bilirubin | 0.4 mg/mL | None Detected |
| Cholesterol | 4.0 mg/mL | None Detected |
| Hemoglobin | 10 mg/mL | None Detected |
| Triglycerides | 15 mg/mL | None Detected |

4. Assay Reportable Range:

Not Applicable.

5. Traceability, Stability, Expected Values (Controls, Calibrators, or Methods):

Not Applicable.

6. Detection Limit:

Not Applicable.

7. Assay Cut-Off:

The cutoff was determined by testing a total of 210 normal sera which consisted of 105 sera from an endemic region of Lyme disease and 105 sera from a non-endemic region of Lyme disease. The mean plus two standard deviations was used to determine the assay cutoff. A known positive sample was then diluted to produce a ready to use cutoff control. An additional 194 samples consisting of 114 samples from different phases of Lyme disease, 8 negative healthy samples, 72 negative Lyme disease samples but do have other diseases that

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may cause serologic cross-reactivity, were tested. A receiver operating characteristics (ROC) analysis was performed to evaluate the performance of the assay and confirm that the chosen cutoff provided the best compromise between sensitivity and specificity.

## B Comparison Studies:

### 1. Method Comparison with Predicate Device:

The Gold Standard Diagnostics *Borrelia burgdorferi* IgG ELISA Test was utilized in a MTTT (2-ELISA) protocol with the Gold Standard Diagnostics *Borrelia burgdorferi* VlsE-OspC IgG/IgM ELISA Test.

The MTTT (2-ELISA) results were compared to the standard two-tier testing (STTT) using the Gold Standard Diagnostics *Borrelia burgdorferi* IgG ELISA followed by testing all positive and equivocal results on the predicate Gold Standard Diagnostics *Borrelia burgdorferi* IgG blot test.

Comparison studies were conducted at three sites (one internal and two external reference laboratories) using prospective samples submitted for Lyme serology testing. Four hundred eighty-one (481) serum samples were tested on the Gold Standard Diagnostics *Borrelia burgdorferi* IgG ELISA Test. A total of 38 positive and equivocal samples were obtained.

In the STTT protocol the samples that were positive or equivocal (n=38) were tested with the predicate B. burgdorferi IgG blot test. In the MTTT protocol the samples (n=38) were tested on a second ELISA, the Gold Standard Diagnostics *Borrelia burgdorferi* VlsE-OspC IgG/IgM ELISA Test. In the second-tier ELISA test, positive and equivocal results were considered positive. These testing strategies are summarized in the two figures below.

Figure 1. STTT-IgG Western Blot Algorithm (WB-STTT [IgG])
Figure 2. MTTT-IgG ELISA Algorithm (ELISA-MTTT [IgG])

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Performance of the second-tier Gold Standard Diagnostics VlsE-OspC IgG/IgM ELISA was also assessed by comparing results to second-tier western blot testing on only those samples positive by the first-tier Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA.

Table 6. Second-tier Performance Summary First-tier Positives Only

| | Predicate WB [IgG] | | | |
| --- | --- | --- | --- | --- |
| | | Positive | Negative | Total |
| Gold Standard Diagnostics VlsE-OspC IgG/IgM ELISA | Positive | 23 | 15 | 38 |
| | Negative | 0 | 0 | 0 |
| Total | | 23 | 15 | 38 |

Positive Percent Agreement: 100% (23/23) 95% CI: 85.2-100%
Negative Percent Agreement: 0% (0/15) 95% CI: 0-21.8%

The results of the MTTT when compared to the STTT are summarized in the following table:

Table 7. Performance Summary - ELISA-MTTT [IgG] compared to WB-STTT [IgG]

| | WB-STTT [IgG] | | | |
| --- | --- | --- | --- | --- |
| | | Positive | Negative | Total |
| Gold Standard Diagnostics ELISA-MTTT [IgG] | Positive | 23 | 15 | 38 |
| | Negative | 0 | 443 | 443 |
| Total | | 23 | 458 | 481 |

Positive Percent Agreement: 100% (23/23) 95% CI: 85.2-100%
Negative Percent Agreement: 96.7% (443/458) 95% CI: 94.7-98.2%

The above performance table artificially inflates the negative percent agreement of the second-tier test since a large number of negatives are negative by the first tier test.

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2. Matrix Comparison:

Not applicable.

C Clinical Studies:

1. Clinical Sensitivity:

Sensitivity Study: A sensitivity study was performed on 125 clinically characterized samples. The samples encompass early, disseminated, and late stages of Lyme disease. The samples were tested on both the Gold Standard Diagnostics MTTT algorithm and the predicate STTT algorithm. The results are summarized in the following table:

Table 8. Sensitivity Study Results - Comparison of ELISA-MTTT [IgG] and WB-STTT [IgG] algorithms

| | N | Gold Standard Diagnostics ELISA-MTTT [IgG] | | Predicate WB-STTT [IgG] | |
| --- | --- | --- | --- | --- | --- |
| Disease Stage | | Positive/Eqv. | % Agreement with Clinical Diagnosis | Positive/Eqv. | % Agreement with Clinical Diagnosis |
| Early | 62 | 30 | 48.4% | 5 | 8.1% |
| Disseminated | 22 | 18 | 81.8% | 5 | 22.7% |
| Late | 41 | 40 | 97.6% | 39 | 95.1% |

CDC Reference Panel: A panel of 280 positive and negative specimens from the Centers of Disease Control (CDC) for Lyme disease detection was tested on both the Gold Standard Diagnostics ELISA-MTTT [IgG] and on the predicate WB-STTT [IgG]. The results are summarized in the following table.

Table 9. CDC Reference Panel Results - Comparison of ELISA-MTTT [IgG] and WB-STTT [IgG] algorithms

| Sample Category | Gold Standard Diagnostics ELISA-MTTT [IgG] | | Predicate WB-STTT [IgG] | |
| --- | --- | --- | --- | --- |
| | Pos. | % Agreement with Clinical Diagnosis | Pos. | % Agreement with Clinical Diagnosis |
| Early Lyme (N = 60) | 36 | 60.0% | 12 | 33.3% |
| Cardiac Lyme (N = 3) | 2 | 66.7% | 1 | 33.3% |
| Neurological Lyme | 6 | 85.7% | 1 | 14.3% |

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| (N = 7) | | | | |
| --- | --- | --- | --- | --- |
| Late Lyme (N = 20) | 20 | 100% | 20 | 100% |
| Healthy Controls (N = 100) | 0 | 100% | 0 | 100% |
| Disease Controls (N = 90) | 0 | 100% | 0 | 100% |

2. Clinical Specificity:

Not Applicable.

3. Other Clinical Supportive Data (When 1. and 2. Are Not Applicable):

Not Applicable.

D Clinical Cut-Off:

Not Applicable.

E Expected Values/Reference Range:

The range of values and positivity rate among different studies and population for the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test are as follows:

Table 10. Expected values of the Gold Standard Diagnostics Borrelia burgdorferi IgG ELISA Test

| Population | # Samples | Unit Results | | | Qualitative Results | |
| --- | --- | --- | --- | --- | --- | --- |
| | | Mean | Range | Std. Dev. | # Positive /Equivocal | % Positive /Equivocal |
| Normal Endemic | 103 | 3.7 | 0.5 – 14.3 | 2.452 | 4 | 3.9% |
| Normal Non-Endemic | 105 | 3.9 | 0.6 – 8.9 | 2.0002 | 0 | 0.0% |
| Prospective Study | 523 | 4.3 | 0.1 – 22.2 | 4.409 | 57 | 10.9% |
| Sensitivity Study | 114 | 13.6 | 0.9 – 40.4 | 7.994 | 81 | 71.1% |

VIII Proposed Labeling:

The labeling supports the finding of substantial equivalence for this device.

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IX Conclusion:

The submitted information in this premarket notification is complete and supports a substantial equivalence decision.

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