MODUILAR UNIPOLAR— 510(k) K950998

Name: FDA 510(k) clearance K950998
Creator: U.S. Food and Drug Administration
Published: 1995-04-13

Substantially Equivalent

Intermedics Orthopedics

FDA 510(k) clearance K950998 for MODUILAR UNIPOLAR, Substantially Equivalent on 1995-04-13. Applicant: Intermedics Orthopedics. Device class: 2.

Clearance details

Applicant: Intermedics Orthopedics
Product code: Code KXA
Device class: Class 2
Regulation: 21 CFR 888.3400
Advisory panel: Orthopedic
Date received: 1995-03-03
Decision date: 1995-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KXA

product code KXA

Injury: 324
Total: 324

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.