SUBTALAR PEG IMPLANT— 510(k) K033046

Substantially Equivalent

Nexa Orthopedics, Inc.

FDA 510(k) clearance K033046 for SUBTALAR PEG IMPLANT, Substantially Equivalent on 2003-12-23. Applicant: Nexa Orthopedics, Inc.. Device class: 2.

Clearance details

Applicant: Nexa Orthopedics, Inc.
Product code: Code MJW
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2003-09-29
Decision date: 2003-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vista, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MJW

K922292 — LUNDEEN SUBTALAR PEG IMPLANT1992-10-23

More clearances from Nexa Orthopedics, Inc.

K072710 — NEXFIX COMPRESSION PIN2007-11-08
K071147 — NEXA ORTHOPEDICS TOTAL SHOULDER SYSTEM2007-07-20
K070688 — NEXFIX COMPRESSION STAPLE2007-05-18
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.