FDA 510(k) clearance · back to tracker

SPY Portable Handheld Imaging (SPY-PHI) System

Novadaq Technologies Ulc (A Part of Stryker) cleared K230727 on 2023-06-05, decision: substantially equivalent

K-number

K230727

Sponsor

Novadaq Technologies Ulc (A Part of Stryker)

Device

SPY Portable Handheld Imaging (SPY-PHI) System

Class

Class II

Decision

Substantially Equivalent

Decision date

2023-06-05

Product code

IZI

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1600

Official FDA record

Open K230727on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K230727 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

Try the sandbox

Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.