VENUS HIP— 510(k) K913708

Name: FDA 510(k) clearance K913708
Creator: U.S. Food and Drug Administration
Published: 1992-01-27

Substantially Equivalent

Turnkey Intergration USA, Inc.

FDA 510(k) clearance K913708 for VENUS HIP, Substantially Equivalent on 1992-01-27. Applicant: Turnkey Intergration USA, Inc.. Device class: 2.

Clearance details

Applicant: Turnkey Intergration USA, Inc.
Product code: Code LWJ
Device class: Class 2
Regulation: 21 CFR 888.3360
Advisory panel: Orthopedic
Date received: 1991-08-16
Decision date: 1992-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LWJ

product code LWJ

Injury: 544
Total: 544

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.