MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM— 510(k) K081883

Name: FDA 510(k) clearance K081883
Creator: U.S. Food and Drug Administration
Published: 2008-09-24

Substantially Equivalent

Us Spine

FDA 510(k) clearance K081883 for MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM, Substantially Equivalent on 2008-09-24. Applicant: Us Spine. Device class: 2.

Clearance details

Applicant: Us Spine
Product code: Code MNH
Device class: Class 2
Regulation: 21 CFR 888.3070
Advisory panel: Orthopedic
Date received: 2008-07-02
Decision date: 2008-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Apple Valley, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MNH

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K162066 — Reliance Spinal Screw System2016-12-02
K162801 — CastleLoc Spinal Fixation System2016-11-03
K162143 — FixxSure® X-Link2016-09-23
K161151 — Spinal fixation system2016-09-21
K162189 — ANAX 5.5 Spinal System2016-08-30

More clearances from Us Spine

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K082801 — PHANTOM PLUS CAGE SYSTEM2008-12-22
K081296 — PREFERENCE PEDICLE SCREW SYSTEM2008-06-06
K062785 — LTD POLYAXIAL FIXATION SYSTEM2006-12-26
K061041 — US SPINE FACET FIXATION SYSTEM2006-06-19

Adverse events under product code MNH

product code MNH

Injury: 978
Malfunction: 793
Total: 1,771

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.