Momentum Spine— 510(k) K232023

Name: FDA 510(k) clearance K232023
Creator: U.S. Food and Drug Administration
Published: 2023-10-04

Substantially Equivalent

Momentum Health, Inc.

FDA 510(k) clearance K232023 for Momentum Spine, Substantially Equivalent on 2023-10-04. Applicant: Momentum Health, Inc.. Device class: Unclassified.

Clearance details

Applicant: Momentum Health, Inc.
Product code: Code LDK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2023-07-07
Decision date: 2023-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.