Skip to content

Estremo Fibular Nail ø3.3x180mm Right

by Citieffe

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08059386742570 UDI-DI Date15 Dec 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Estremo Fibular Nail
Generic Name
Arthrodesis intramedullary nail, non-distracting
Model / Ref / Catalog
Estremo Fibular Nail ø3.3x180mm Right, FN03318R
Primary DI / UDI-DI
08059386742570
510(k) Number
FDA Product Code
HSB
GMDN Term
Arthrodesis intramedullary nail, non-distracting
Device Class
Class II
Regulation Number
888.3020
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250197)

Show all (12)

Other devices from Citieffe

See all devices from Citieffe →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No