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Cannulated Fully Threaded Cancellous Screw, Reduced Head 8502-48-026

by Biomet Orthopedics, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887868053474 UDI-DI Date24 Oct 2015ListedStatusListed 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  • Withdrawn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
Cannulated Fully Threaded Cancellous Screw, Reduced Head
Generic name
Orthopaedic bone screw, non-bioabsorbable, sterile
Model / Ref / Catalog
8502-48-026, 850248026
Primary DI / UDI-DI
00887868053474
FDA product code
KTT, JDW, LXT, HTY, HTN, HSB, HWC, HRS
GMDN term
Orthopaedic bone screw, non-bioabsorbable, sterile
Device class
Class II
Regulation number
888.3030, 888.3040, 888.3020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (10)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No