VERTA Corpectomy Cage— 510(k) K143490

Name: FDA 510(k) clearance K143490
Creator: U.S. Food and Drug Administration
Published: 2015-01-26

Substantially Equivalent

Camber Spine

FDA 510(k) clearance K143490 for VERTA Corpectomy Cage, Substantially Equivalent on 2015-01-26. Applicant: Camber Spine. Device class: 2.

Clearance details

Applicant: Camber Spine
Product code: Code MQP
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2014-12-08
Decision date: 2015-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, PA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Camber Spine

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K133366 — ORTHROS POSTERIOR STABILIZATION SYSTEM2014-04-08
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K134038 — CAMBER SPINE DIAGON OBLIQUE CAGE2014-03-20

Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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