RELIANCE SPINAL SCREW SYSTEM— 510(k) K101112

Name: FDA 510(k) clearance K101112
Creator: U.S. Food and Drug Administration
Published: 2010-11-04

Substantially Equivalent

Reliance Medical Systems

FDA 510(k) clearance K101112 for RELIANCE SPINAL SCREW SYSTEM, Substantially Equivalent on 2010-11-04. Applicant: Reliance Medical Systems. Device class: 2.

Clearance details

Applicant: Reliance Medical Systems
Product code: Code KWP
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2010-04-21
Decision date: 2010-11-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Bountiful, UT, US

Download summary PDF View on FDA.gov ↗

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K150753 — OASYS System2015-06-09
K150851 — Sure Lok Mini Posterior Cervical/Upper Thoracic System2015-06-04
K142867 — Reliance Posterior Cervical-Thoracic System2015-04-29
K150254 — Streamline OCT Occipito-Cervico-Thoracic System2015-04-28

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K181118 — Reliance Lumbar IBF System2019-01-09
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Adverse events under product code KWP

product code KWP

Death: 7
Injury: 1,539
Malfunction: 1,519
Total: 3,065

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.