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Moss Miami Spinal System (Anterior Use)

by Depuy, Inc. 510(k)

Active United States

510(k) K953915

Overview

The Moss Miami Spinal System (Anterior Use) is a spinal implant system intended for non-cervical use in the spine. It is designed to be used with anterior screw fixation or posterior hook, non-pedicle screw fixation.

It is indicated for the treatment of scoliosis, kyphosis, lordosis, fracture, loss of stability due to tumor, spinal stenosis, spondylolisthesis, previously failed fusion surgery, or degenerative disc disease. The system received FDA 510(k) clearance under K953915 on February 15, 1996, and is classified under product code MNH with advisory committee review in Orthopedics (OR).

AI-generated from registry data, 19 Sep 2026.Not verified by deviCERTS or the manufacturer

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK953915 Date15 Feb 1996DecidedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
MNH
Device Class
Class II
Regulation
21 CFR Part 888.3070
Advisory Committee
Orthopedic
FDA Decision
SN

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