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CrossRoads Screw System

by Crossroads Extremity Systems LLC 5 variants

CrossRoads Screw System (1456-4040) is a Class I device made by Crossroads Extremity Systems LLC, listed in FDA GUDID since 7 Mar 2016 (UDI-DI 00850310006861), 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 Number00850310006861 UDI-DI Date7 Mar 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  • Withdrawn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
Surgical screwdriver, single-use
Model / Ref / Catalog
4.0 Headed Implant Prep Kit Including Reamer, 1456-4040
Primary DI / UDI-DI
00850310006861
FDA product code
LXH
GMDN term
Surgical screwdriver, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical instrument handle, non-torque-limitingFluted surgical drill bit, single-useOrthopaedic intraoperative positioning pin, single-useSurgical screwdriver, single-use

Similar devices in this category

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)