MODIFICATION TO: INTERPLATE VBR SYSTEM— 510(k) K071372

Name: FDA 510(k) clearance K071372
Creator: U.S. Food and Drug Administration
Published: 2007-06-11

Substantially Equivalent

Rsb Spine, LLC

FDA 510(k) clearance K071372 for MODIFICATION TO: INTERPLATE VBR SYSTEM, Substantially Equivalent on 2007-06-11. Applicant: Rsb Spine, LLC. Device class: 2.

Clearance details

Applicant: Rsb Spine, LLC
Product code: Code MQP
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2007-05-16
Decision date: 2007-06-11
Decision: Substantially Equivalent
Clearance type: Special
Location: Chesterland, OH, US

Download summary PDF View on FDA.gov ↗

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K071922 — INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC2007-09-18
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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.