510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K984350Substantially Equivalent

Vsp System

Depuy Motech Acromed, Cleveland OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K984350 is the FDA 510(k) clearance record for VSP SYSTEM, a class II device, cleared for Depuy Motech Acromed on under FDA product code MNI (Orthosis, Spinal Pedicle Fixation). FDA records list 4 510(k) clearances for Depuy Motech Acromed, from to . As of , FDA records show no recalls naming K984350.

Clearance record

Decision date
Received
(47 days to decision)
Product code
MNI Orthosis, Spinal Pedicle Fixation
Regulation
21 CFR 888.3070
Device class
Class II
Review panel
Orthopedic
Applicant
Depuy Motech Acromed 3303 Carnegie Ave., Cleveland OH
510(k) summary
Summary
Third party review
No

Clearances, product code MNI

Trailing 12 months

FDA records hold no clearances under product code MNI in the trailing twelve months.

FDA records show no clearances under product code MNI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MNI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260