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Minuteman 20-0218-000

by Spinal Simplicity, LLC

Minuteman 20-0218-000 is a Class I device made by Spinal Simplicity, LLC, listed in FDA GUDID since 5 May 2026 (UDI-DI M9432002180000), 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 NumberM9432002180000 UDI-DI Date5 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Minuteman
Generic name
Bone file/rasp, manual, reusable
Model / reference
20-0218-000
Primary DI / UDI-DI
M9432002180000
FDA product code
LXH
GMDN term
Bone file/rasp, manual, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code LXH (Orthopedic Manual Surgical Instrument).

Other devices from Spinal Simplicity, LLC

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Properties

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