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Fusion Posterior Instrument Set 720-418

by Rti Surgical, Inc.

Fusion Posterior Instrument Set 720-418 is a Class I device made by Rti Surgical, Inc., listed in FDA GUDID since 25 Sep 2020 (UDI-DI 00191083025728), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00191083025728 UDI-DI Date25 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fusion Posterior Instrument Set
Generic name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
720-418
Primary DI / UDI-DI
00191083025728
FDA product code
HXG
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General internal orthopaedic fixation system implantation kit

Other devices from Rti Surgical, Inc.

See all devices from Rti Surgical, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)