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Continuum® Trilogy® 00-8791-038-00

by Zimmer, Inc.

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 Number00889024152496 UDI-DI Date19 Jul 2016ListedStatusListed 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  • Withdrawn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
Continuum® Trilogy®
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable
Model / Ref / Catalog
00-8791-038-00
Primary DI / UDI-DI
00889024152496
510(k) Number
FDA Product Code
LPH, LZO, JDI
GMDN Term
Acetabulum prosthesis trial, prefabricated, reusable
Device Class
Class II
Regulation Number
888.3358, 888.3353, 888.3350
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Outer Diameter — 38 Millimeter

Related devices

Category: Acetabulum prosthesis trial, prefabricated, reusable

Cleared under the same submission (K103662)

Show all (12)

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single 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
  • Expiration Date: No
  • Manufacturing Date: No