Skip to content

606.217

by Globus Medical, Inc.

606.217 is a Class I device made by Globus Medical, Inc., listed in FDA GUDID since 17 Feb 2016 (UDI-DI 00849044046724), 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 Number00849044046724 UDI-DI Date17 Feb 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  • Withdrawn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
Spinal implant trial
Model / reference
606.217
Primary DI / UDI-DI
00849044046724
FDA product code
LXH
GMDN term
Spinal implant trial
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Height — 17 Millimeter

Related devices

Category: Spinal implant trial

Other devices from Globus Medical, Inc.

See all devices from Globus Medical, Inc. →

Properties

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