510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K230727Substantially Equivalent

SPY Portable Handheld Imaging (SPY-PHI) System

Novadaq Technologies ULC (A Part of Stryker), Burnaby, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K230727 is the FDA 510(k) clearance record for SPY Portable Handheld Imaging (SPY-PHI) System, a class II device, cleared for Novadaq Technologies Ulc (A Part of Stryker) on under FDA product code IZI (System, X-Ray, Angiographic). FDA records list one 510(k) clearance for Novadaq Technologies Ulc (A Part of Stryker). As of , FDA records show no recalls naming K230727.

Clearance record

Decision date
Received
(81 days to decision)
Product code
IZI System, X-Ray, Angiographic
Regulation
21 CFR 892.1600
Device class
Class II
Review panel
Radiology
Applicant
Novadaq Technologies Ulc (A Part of Stryker) 8329 Eastlake Dr. Unit 101, Burnaby, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IZI

Trailing 12 months
2 clearances under product code IZI in the twelve months to October 2026, May 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IZI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20262
June 20260
July 20260
August 20260
September 20260
October 20260