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Medtronic Resuable Instruments EX0517086

by Medtronic Sofamor Danek, Inc.

Medtronic Resuable Instruments EX0517086 is a Class I device made by Medtronic Sofamor Danek, Inc., listed in FDA GUDID since 8 Sep 2022 (UDI-DI 00763000011192), 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 Number00763000011192 UDI-DI Date8 Sep 2022ListedStatusListed 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  • Withdrawn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
Medtronic Resuable Instruments
Generic name
Surgical drill guide, reusable
Model / reference
EX0517086
Primary DI / UDI-DI
00763000011192
FDA product code
FZX
GMDN term
Surgical drill guide, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical drill guide, reusable

Similar devices in this category

Other devices filed under Surgical drill guide, reusable.

Other devices from Medtronic Sofamor Danek, Inc.

See all devices from Medtronic Sofamor Danek, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)