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Vector Targeting System

by Vector Medical, Inc.

510(k) K022225

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK022225 Date25 Jul 2002ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
Vector Medical, Inc., Vector Targeting System
510(k) Number
FDA Product Code
HSB
Device Class
Class II
Regulation
21 CFR Part 888.3020
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Vector Targeting System is a medical device designed for locating and targeting screw holes in an intramedullary nail. It assists surgeons in identifying the precise position of these holes during orthopedic procedures.

This device is identified by FDA 510(k) number K022225. It is manufactured by Vector Medical, Inc. and is classified under product code HSB.

Other devices from Vector Medical, Inc.

Questions

AI-generated answers, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary function of the Vector Targeting System?

    The Vector Targeting System is designed to assist surgeons during orthopedic procedures by locating and targeting screw holes within an intramedullary nail, ensuring precise positioning.

  • What is the regulatory status of this device?

    The Vector Targeting System is cleared under FDA 510(k) number K022225. It is classified under product code HSB and was determined to be substantially equivalent to existing devices.

  • Who is the manufacturer of the Vector Targeting System?

    The device is manufactured by Vector Medical, Inc., located in Milton, Florida. The company is the official applicant for the device's 510(k) clearance.