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Accolade 1059-6713

by Howmedica Osteonics Corp.

Accolade 1059-6713 is a Class II device made by Howmedica Osteonics Corp., listed in FDA GUDID since 24 Sep 2015 (UDI-DI 07613327014334), 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 Number07613327014334 UDI-DI Date24 Sep 2015ListedStatusListed 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  • Withdrawn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

Trade name
Accolade
Generic name
Orthopaedic cement spacer
Model / Ref / Catalog
1059-6713
Primary DI / UDI-DI
07613327014334
FDA product code
LZO, MEH, KWL, LWJ, MAY, LPH, MBL, KWY, JDI, KWZ
GMDN term
Orthopaedic cement spacer
Device class
Class II
Regulation number
888.3353, 888.3360, 888.3358, 888.3390, 888.3350, 888.3310
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 13.0 Millimeter

Related devices

Category: Orthopaedic cement spacer

Other devices from Howmedica Osteonics Corp.

See all devices from Howmedica Osteonics Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)