Spine CAMP (1.1)— 510(k) K231668

Substantially Equivalent

Medical Metrics, Inc.

FDA 510(k) clearance K231668 for Spine CAMP (1.1), Substantially Equivalent on 2023-07-07. Applicant: Medical Metrics, Inc.. Device class: 2.

Clearance details

Applicant: Medical Metrics, Inc.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2023-06-07
Decision date: 2023-07-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QIH

K260879 — 4DM2026-09-10
K261795 — Quicktome Software Suite2026-09-10
K251417 — ReVISION 22026-09-09
K260525 — NextMR Spine2026-09-04
K260811 — Heartvue.Proton2026-08-26

More clearances from Medical Metrics, Inc.

K221632 — Spine CAMP2022-10-18
K022585 — KIMAX QMA2002-10-11
K013098 — KIMAX REMOTE VIEWING STATION2001-12-07
K010187 — KIMAX, MODEL 10242001-02-14

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