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9734149

by Medtronic Navigation Inc.

9734149 is a Class II device made by Medtronic Navigation Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00613994570352), 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 Number00613994570352 UDI-DI Date19 Sep 2016ListedStatusListed 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  • Withdrawn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
Orthopaedic stereotactic surgery system
Model / reference
9734149
Primary DI / UDI-DI
00613994570352
FDA product code
HAW
GMDN term
Orthopaedic stereotactic surgery system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic stereotactic surgery system

Similar devices in this category

Other devices filed under Orthopaedic stereotactic surgery system.

Other devices from Medtronic Navigation Inc.

See all devices from Medtronic Navigation Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)