PRESS-FIT HIP STEM— 510(k) K964178

Name: FDA 510(k) clearance K964178
Creator: U.S. Food and Drug Administration
Published: 1997-05-05

Substantially Equivalent

Encore Orthopedics, Inc.

FDA 510(k) clearance K964178 for PRESS-FIT HIP STEM, Substantially Equivalent on 1997-05-05. Applicant: Encore Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Encore Orthopedics, Inc.
Product code: Code LWJ
Device class: Class 2
Regulation: 21 CFR 888.3360
Advisory panel: Orthopedic
Date received: 1996-10-18
Decision date: 1997-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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K082146 — METHA SHORT STEM HIP SYSTEM XL FEMORAL HEAD2008-09-09
K070061 — 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT2007-01-31

More clearances from Encore Orthopedics, Inc.

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K032905 — 3DKNEE POROUS COATED FEMORAL COMPONENT2004-07-06
K020114 — 3D KNEE2002-07-12
K020741 — UNICONDYLAR KNEE2002-06-04
K020236 — MODIFICATION TO PASS SPINAL SYSTEM2002-02-14
K020170 — KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP2002-02-11

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.