NEXA CARPO METACARPAL IMPLANT— 510(k) K060386

Name: FDA 510(k) clearance K060386
Creator: U.S. Food and Drug Administration
Published: 2006-05-10

Substantially Equivalent

Nexa Orthopedics, Inc.

FDA 510(k) clearance K060386 for NEXA CARPO METACARPAL IMPLANT, Substantially Equivalent on 2006-05-10. Applicant: Nexa Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Nexa Orthopedics, Inc.
Product code: Code KYI
Device class: Class 2
Regulation: 21 CFR 888.3770
Advisory panel: Orthopedic
Date received: 2006-02-14
Decision date: 2006-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.