K141397

Substantially Equivalent

SURE-LOK C EXTENDED TAB PEDICLE SCREW SYSTEM

Applicant: Precision Spine, Inc.
Product code: MNI
Advisory panel: Orthopedic
Date received: 2014-05-28
Decision date: 2014-06-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Pear, MS, US

Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.