ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL— 510(k) K120143

Name: FDA 510(k) clearance K120143
Creator: U.S. Food and Drug Administration
Published: 2012-02-16

Substantially Equivalent

Apollo Spine

FDA 510(k) clearance K120143 for ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL, Substantially Equivalent on 2012-02-16. Applicant: Apollo Spine. Device class: 2.

Clearance details

Applicant: Apollo Spine
Product code: Code ODP
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2012-01-18
Decision date: 2012-02-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Newbury, NH, US

Download summary PDF View on FDA.gov ↗

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K254130 — C.A. Medical Interbody Fusion System2026-07-08

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.