BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - TICARCILLIN (GN) 1-128 UG/ML

K062680 · Becton, Dickinson & CO · LON · Oct 5, 2006 · Microbiology

Device Facts

• Record ID: K062680
• Device Name: BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - TICARCILLIN (GN) 1-128 UG/ML
• Applicant: Becton, Dickinson & CO
• Product Code: LON · Microbiology
• Decision Date: Oct 5, 2006
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 866.1645
• Device Class: Class 2

Intended Use

Ticarcillin at 1 – 128 µg/mL on the GN ID/AST or AST only Phoenix panels is intended for use with the BD Phoenix Automated Microbiology System for in vitro quantitative determination of antimicrobial susceptibility by minimal inhibitory concentration (MIC) of most Gram-negative aerobic and facultative anaerobic bacteria isolates from pure culture for Enterobacteriaceae and non–Enterobacteriaceae and most Gram-positive bacteria isolates from pure culture belonging to the genera Staphylococcus, Enterococcus, and Streptococcus.

Device Story

BD Phoenix System performs automated identification and antimicrobial susceptibility testing (AST) of bacterial isolates. Input: pure culture bacterial isolates inoculated into sealed, molded polystyrene panels containing biochemicals and antimicrobial agents. Operation: instrument incubates panels at 35°C; optical sensors measure redox indicator changes and bacterial turbidity every 20 minutes. Output: organism identification, MIC values, and categorical interpretations (S, I, R). Used in clinical microbiology laboratories by trained technicians. Results assist clinicians in selecting appropriate antibiotic therapy for patients with bacterial infections.

Clinical Evidence

Performance evaluated using clinical, stock, and challenge isolates across multiple U.S. sites. Results compared to CLSI reference broth microdilution method. Metrics included Essential Agreement (EA) and Category Agreement (CA). Study demonstrated substantial equivalence to reference methods for Gram-negative panels containing ticarcillin.

Technological Characteristics

Automated microbiology system; broth microdilution principle; redox indicator for growth detection; molded polystyrene panels (136 micro-wells); incubation at 35°C; optical turbidity/redox measurement; software-based interpretation of MIC and categorical results.

Indications for Use

Indicated for ticarcillin susceptibility testing of Gram-negative aerobic/facultative anaerobic bacteria (Enterobacteriaceae and non-Enterobacteriaceae) and Gram-positive bacteria (Staphylococcus, Enterococcus, Streptococcus) from pure culture. This application specifically removes the limitation for Proteus vulgaris/penneri.

Regulatory Classification

Identification

A fully automated short-term incubation cycle antimicrobial susceptibility system is a device that incorporates concentrations of antimicrobial agents into a system for the purpose of determining in vitro susceptibility of bacterial pathogens isolated from clinical specimens. Test results obtained from short-term (less than 16 hours) incubation are used to determine the antimicrobial agent of choice to treat bacterial diseases.

Special Controls

*Classification.* Class II (special controls). The special control for this device is FDA's guidance document entitled “Class II Special Controls Guidance Document: Antimicrobial Susceptibility Test (AST) Systems; Guidance for Industry and FDA.”

Predicate Devices

• VITEK® System (PMA No. N50510)
• BD Phoenix™ Automated Microbiology System with Gatifloxacin (K020321)
• Ticarcillin (K031984)
• Ticarcillin (K061327)

Submission Summary (Full Text)

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510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION
DECISION SUMMARY
ASSAY ONLY TEMPLATE

A. 510(k) Number:
k062680

B. Purpose for Submission:
To remove limitation of Proteus vulgaris/penneri with ticarcillin on the Gram-Negative (GN) ID/AST or AST only Phoenix panels

C. Measurand:
Ticarcillin 1 – 128 µg/mL

D. Type of Test:
Antimicrobial Susceptibility Test (AST) colorimetric oxidation-reduction, growth-based

E. Applicant:
Becton, Dickinson & Company

F. Proprietary and Established Names:
BD Phoenix™ Automated Microbiology System – Ticarcillin 1 – 128 µg/mL

G. Regulatory Information:

1. Regulation section:
21 CFR 866.1645 Fully Automated Short-Term Incubation Cycle Antimicrobial Susceptibility System

2. Classification:
II

3. Product code:
LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

4. Panel:
83 Microbiology

H. Intended Use:

1. Intended use(s):
Ticarcillin at 1 – 128 µg/mL on the GN ID/AST or AST only Phoenix panels is intended for use with the BD Phoenix Automated Microbiology System for in vitro quantitative determination of antimicrobial susceptibility by minimal inhibitory concentration (MIC) of most Gram-negative aerobic and facultative

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anaerobic bacteria isolates from pure culture for Enterobacteriaceae and non–Enterobacteriaceae and most Gram-positive bacteria isolates from pure culture belonging to the genera Staphylococcus, Enterococcus, and Streptococcus.

2. Indication(s) for use:
This application is indicated for ticarcillin for the removal of limitation for Proteus vulgaris/penneri.

3. Special conditions for use statement(s):
For prescription use only

4. Special instrument requirements:
Not Applicable

I. Device Description:

This submission is for AST Panel only. The ID System was not reviewed.

The BD Phoenix™ Automated Microbiology System includes instrumentation and software, sealed and self-inoculating molded polystyrene trays with 136 micro-wells containing dried reagents, and specific inoculum broth formulations for ID and AST Indicator. The organism to be tested must be a pure culture and be preliminarily identified as gram positive or gram negative. Colonies are then suspended in broth, and equated to a 0.5 McFarland with the recommendation to use the BD CrystalSpec™ Nephelometer. A further dilution is made into an AST broth, which contains an AST indicator, prior to inoculating the panel. The AST broth is a cation-adjusted formulation of Mueller-Hinton broth containing 0.01% Tween 80. After adding the indicator solution to the AST inoculum the color is blue and after inoculation and incubation changes to pink then to colorless as reduction in the panel well proceeds. Inoculated panels are barcode scanned and loaded into the BD Phoenix™ Automated Microbiology System instrument where the panels are continuously incubated at 35°C. The AST has a final inoculum of 5 × 10⁵ CFU/ml. The instrument incubates, reads and records the results of the biochemical substrates and antimicrobial agents and interprets the reactions to give an ID of the isolate and MIC value and category interpretation of the antimicrobial agents. Organisms growing in the presence of a given antimicrobic agent reduce the indicator, signaling organism growth and resistance to the antimicrobic agent. Organisms killed or inhibited by a given antimicrobic do not cause reduction of the indicator and therefore do not produce a color change. Additional interpretation is done using software driven "EXPERT" System using rules derived from the CLSI documentation.

Readings are taken every 20 minutes with an AST result available between 4-16 hours. This is only an autoread result; no manual readings are possible with this system.

J. Substantial Equivalence Information:

1. Predicate device name(s):

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VITEK® System

2. Predicate 510(k) number(s):
N50510

3. Comparison with predicate:

| Similarities | | |
| --- | --- | --- |
| Item | Device | Predicate |
| 1. Intended Use | Intended for the in vitro rapid identification (ID) and quantitative determination of antimicrobial susceptibility by minimal inhibitory concentration (MIC) of most bacteria. | Same |
| 2. Isolates | Isolated colonies from culture used | Isolated colonies from culture used |
| 3. Result Reported | Report results as minimum inhibitory concentration (MIC) and categorical interpretation (SIR) | Report results as minimum inhibitory concentration (MIC) and categorical interpretation (SIR) |
| 4. Incubation Time | <16 hours | <16 hours |
| 5. Type of Test | Automated | Automated |
| Differences | | |
| --- | --- | --- |
| Item | Device | Predicate |
| 1. Results achieved | Results are determined from serial twofold dilutions of antimicrobial agents | Results are determined from extrapolation of doubling dilutions |
| 2. Sample Preparation | Inoculum density equated to 0.5 McFarland standard | Inoculum density equated to 1.0 McFarland standard |
| 3. Technology | Automated growth based enhanced by use of a redox indicator (colorimetric oxidation-reduction) to detect organism growth. | Automated growth based with detection using an attenuation of light measured by an optical scanner. |

K. Standard/Guidance Document Referenced (if applicable):
"Class II Special Controls Guidance Document: Antimicrobial Susceptibility Test Systems; Guidance for Industry and FDA"; CLSI M7 (M100-S16) "Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically;

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Approved Standard."

L. Test Principle:
The AST portion of the BD Phoenix™ Automated Microbiology System is a broth based microdilution method that utilizes a redox indicator (colorimetric oxidation-reduction) to enhance detection of organism growth. The MIC is determined by comparing growth in wells containing serial two-fold dilutions of an antibiotic to the growth in “growth control wells” which contains no antibiotic.

M. Performance Characteristics (if/when applicable):

1. Analytical performance:
The data included in this submission were acquired during the clinical studies performed at multiple sites and described in the previous submission for Ticarcillin 1 – 128 µg/ml. The accuracy performance data using ID specific algorithm for clinical and challenge isolates of Proteus vulgaris/penneri and ticarcillin are contained in this submission. The Reproducibility study was performed in the previous submission (k031984) and was not performed for this submission because the drug formulation has not changed. The QC performance was within the expected ranges as shown under the “Traceability, Stability... section (c)”.

a. Precision/Reproducibility:
Intersite and Intrasite testing demonstrated &gt;95% reproducibility. The ten isolate study described in the guidance document was used (10 organisms tested 3 times on 3 days at 3 sites).

b. Linearity/assay reportable range:
Not applicable

c. Traceability, Stability, Expected values (controls, calibrators, or methods):
Quality Control was performed on every test occasion with the following results. BD Phoenix™ produced acceptable QC results as compared to the reference method results &gt;95% of the time.

Ticarcillin QC Table
| ORGANISM | conc. (µg/mL) | Reference | | BD Phoenix™ | | |
| --- | --- | --- | --- | --- | --- | --- |
| | | | | | | |
| E. cloacae ATCC 11061
Expected Range : ≥64 µg/mL | >128 | | 49 | | 69 | |
| | | | | | | |
| | | | | | | |
| E. coli
ATCC 25922
Expected Range :
4 - 16 µg/mL | 2 | | 1 | | | |
| | 4 | | 22 | | | |
| | 8 | | 17 | | 35 | |
| | 16 | | 8 | | 34 | |

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| | | | | | | |
| --- | --- | --- | --- | --- | --- | --- |
| E. coli
ATCC 35218
Expected Range :
≥128 μg/mL | 2 | | 1 | | 1 | |
| | 4 | | | | | |
| | 8 | | | | | |
| | 16 | | | | | |
| | 32 | | | | | |
| | 64 | | | | | |
| | 128 | | | | | |
| | >128 | | 48 | | 68 | |
| | | | | | | |
| P. aeruginosa
ATCC 27853
Expected Range :
8 - 32 μg/mL | 8 | | 1 | | | |
| | 16 | | 41 | | 7 | |
| | 32 | | 5 | | 61 | |
| | 64 | | 1 | | | |
| | | | | | | |

Inoculum density control: The organism suspension density of the ID broth was equivalent to a 0.5 McFarland standard using the BBL™ CrystalSpec™ Nephelometer which was verified each day of testing. Internal data was used to demonstrate that the use of the BBL™ CrystalSpec™ Nephelometer would produce reproducible results. Five different instruments were used.

d. Detection limit:
Not Applicable

e. Analytical specificity:
Not Applicable

f. Assay cut-off:
Not Applicable

2. Comparison studies:

a. Method comparison with predicate device:
The broth dilution reference panel was prepared according to the CLSI recommendation and used to compare with the BD Phoenix™ results. Clinical testing was performed at several sites. The testing included both fresh clinical isolates and stock isolates along with a challenge set with known results. A total of 80 Proteus vulgaris/penneri isolates were tested with acceptable EA and no maj or very maj errors. Additionally, 466 clinical strains related appropriate groups were tested to demonstrate that there would be no difference in performance from the original studies. The following table includes the overall performance of all appropriate organisms tested.

GN Accuracy Summary Clinical and Challenge with ID Specific Algorithm for Proteus vulgaris/penneri

| | EA Tot | EA N | EA % | Eval EA Tot | Eval EA N | Eval EA % | CA N | CA % | #R | min | maj | vmj |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Combined | 3428 | 3254 | 94.9 | 1512 | 1391 | 92 | 3190 | 93.1 | 1670 | 162 | 59 | 17 |

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EA-Essential Agreement
vmj – very major discrepancies
CA-Category Agreement
maj - major discrepancies
R-resistant isolates
min – minor discrepancies

Essential agreement (EA) is when the BD Phoenix™ panels agree with the reference test panel results exactly or within one doubling dilution of the reference method. Category agreement (CA) is when the BD Phoenix™ panel result interpretation (SIR) agrees exactly with the reference panel result interpretation. Evaluable EA is when the MIC result is on scale for both the BD Phoenix™ and the reference and have on-scale EA.

b. Matrix comparison:
Not Applicable

3. Clinical studies:
a. Clinical Sensitivity:
Not Applicable
b. Clinical specificity:
Not Applicable
c. Other clinical supportive data (when a. and b. are not applicable):
Not Applicable

4. Clinical cut-off:
Not Applicable

5. Expected values/Reference range:
Enterobacteriaceae ≤16 (S); 32 – 64 (I); ≥128(R)
Pseudomonas aeruginosa ≤64 (S); ≥128(R)
Other Non – Enterobacteriaceae ≤16 (S); 32 – 64 (I); ≥128(R)

N. Proposed Labeling:
The expected value range, interpretive criteria and QC for gram negative panels are included in the package insert. The labeling is sufficient and satisfies the requirements of 21 CFR Part 809.10.

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