ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY— 510(k) K063251

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K063251 for ZIMMER M/L TAPER HIP PROSTHESIS WITH MODULAR NECK TECHNOLOGY, Substantially Equivalent on 2007-01-24. Applicant: Zimmer, Inc..

Clearance details

Applicant: Zimmer, Inc.
Product code: Code KWA
Advisory panel: Orthopedic
Date received: 2006-10-27
Decision date: 2007-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code KWA

product code KWA

Death: 38
Injury: 10,439
Malfunction: 1,862
Total: 12,339

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.