ShurFit 2C Lumbar Interbody Fusion System— 510(k) K171657

Name: FDA 510(k) clearance K171657
Creator: U.S. Food and Drug Administration
Published: 2017-08-11

Substantially Equivalent

Precision Spine, Inc.

FDA 510(k) clearance K171657 for ShurFit 2C Lumbar Interbody Fusion System, Substantially Equivalent on 2017-08-11. Applicant: Precision Spine, Inc.. Device class: 2.

Clearance details

Applicant: Precision Spine, Inc.
Product code: Product code MAX
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2017-06-05
Decision date: 2017-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pear, MS, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MAX

product code MAX

Death: 13
Injury: 1,305
Malfunction: 2,885
Total: 4,203

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.