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Minuteman 20-0096-014

by Spinal Simplicity, LLC

Minuteman 20-0096-014 is a Class I device made by Spinal Simplicity, LLC, listed in FDA GUDID since 26 Jul 2024 (UDI-DI M9432000960140), 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 NumberM9432000960140 UDI-DI Date26 Jul 2024ListedStatusListed 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  • Withdrawn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
Orthopaedic implant-instrument extension adaptor, reusable
Model / reference
20-0096-014
Primary DI / UDI-DI
M9432000960140
FDA product code
LXH
GMDN term
Orthopaedic implant-instrument extension adaptor, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant-instrument extension adaptor, reusable

Similar devices in this category

Other devices filed under Orthopaedic implant-instrument extension adaptor, reusable.

Other devices from Spinal Simplicity, LLC

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Properties

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