SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM— 510(k) K980288

Substantially Equivalent for Some Indications

Spine-Tech, Inc.

FDA 510(k) clearance K980288 for SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM, Substantially Equivalent for Some Indications on 1998-07-29. Applicant: Spine-Tech, Inc..

Clearance details

Applicant: Spine-Tech, Inc.
Product code: Code KWP
Advisory panel: Orthopedic
Date received: 1998-01-26
Decision date: 1998-07-29
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Minneapolis, MN, US

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Adverse events under product code KWP

product code KWP

Death: 7
Injury: 1,539
Malfunction: 1,519
Total: 3,065

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.