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9731833

by Medtronic Navigation Inc. 2 variants

9731833 is a Class II device made by Medtronic Navigation Inc., listed in FDA GUDID since 3 Mar 2019 (UDI-DI 00763000055943), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00763000055943 UDI-DI Date3 Mar 2019ListedStatusListed 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  • Withdrawn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

Generic name
Multi-purpose stereotactic surgery system
Model / reference
9731833
Primary DI / UDI-DI
00763000055943
FDA product code
HAW
GMDN term
Multi-purpose stereotactic surgery system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Multi-purpose stereotactic surgery system

Similar devices in this category

Other devices filed under Multi-purpose stereotactic surgery system.

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)