CONSENSUS(TM) HIP SYSTEM-HA COATED TIANIUM FEM STEM— 510(k) K935453

Name: FDA 510(k) clearance K935453
Creator: U.S. Food and Drug Administration
Published: 1994-07-13

Substantially Equivalent for Some Indications

U.S. Medical Products, Inc.

FDA 510(k) clearance K935453 for CONSENSUS(TM) HIP SYSTEM-HA COATED TIANIUM FEM STEM, Substantially Equivalent for Some Indications on 1994-07-13. Applicant: U.S. Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: U.S. Medical Products, Inc.
Product code: Code MEH
Device class: Class 2
Regulation: 21 CFR 888.3353
Advisory panel: Orthopedic
Date received: 1993-11-12
Decision date: 1994-07-13
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MEH

product code MEH

Injury: 2,021
Total: 2,021

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.