MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM— 510(k) K992276

Substantially Equivalent

Sulzer Spine-Tech

FDA 510(k) clearance K992276 for MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM, Substantially Equivalent on 1999-10-01. Applicant: Sulzer Spine-Tech.

Clearance details

Applicant: Sulzer Spine-Tech
Product code: Code MNI
Advisory panel: Orthopedic
Date received: 1999-07-07
Decision date: 1999-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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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.