HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS— 510(k) K022463

Name: FDA 510(k) clearance K022463
Creator: U.S. Food and Drug Administration
Published: 2002-08-16

Substantially Equivalent

Biomet Orthopedics, Inc.

FDA 510(k) clearance K022463 for HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS, Substantially Equivalent on 2002-08-16. Applicant: Biomet Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Biomet Orthopedics, Inc.
Product code: Product code LPH
Device class: Class 2
Regulation: 21 CFR 888.3358
Advisory panel: Orthopedic
Date received: 2002-07-26
Decision date: 2002-08-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LPH

product code LPH

Death: 73
Injury: 31,640
Malfunction: 3,358
Other: 2
Total: 35,073

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.