FDA 510(k) clearance · back to tracker

Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 Family

Siemens Medical Solutions USA, Inc. cleared K261315 on 2026-05-21, decision: substantially equivalent

K-number

K261315

Sponsor

Siemens Medical Solutions USA, Inc.

Device

Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 Family

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-05-21

Product code

KPS

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.1200

Official FDA record

Open K261315on 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 K261315 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.