FDA 510(k) clearance · back to tracker

POSEIDON ST

Signus Medinzintechnik GmbH cleared K261031 on 2026-07-10, decision: substantially equivalent

K-number

K261031

Sponsor

Signus Medinzintechnik GmbH

Device

POSEIDON ST

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-07-10

Product code

MQP

Advisory committee

Orthopedic

Medical specialty

Orthopedic

Regulation number

888.3060

Official FDA record

Open K261031on 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.

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Source

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