MODIFICATION TO CLASSIC GREAT TOE IMPLANT— 510(k) K023562

Name: FDA 510(k) clearance K023562
Creator: U.S. Food and Drug Administration
Published: 2002-11-13

Substantially Equivalent

Nexa Orthopedics, Inc.

FDA 510(k) clearance K023562 for MODIFICATION TO CLASSIC GREAT TOE IMPLANT, Substantially Equivalent on 2002-11-13. Applicant: Nexa Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Nexa Orthopedics, Inc.
Product code: Code KWH
Device class: Class 2
Regulation: 21 CFR 888.3720
Advisory panel: Orthopedic
Date received: 2002-10-23
Decision date: 2002-11-13
Decision: Substantially Equivalent
Clearance type: Special
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

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K060386 — NEXA CARPO METACARPAL IMPLANT2006-05-10
K060071 — NEXA COMPRESSION SCREW2006-01-26

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