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Delta Xtend 1337-66-042

by Depuy (Ireland)

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 Number10603295523161 UDI-DI Date24 Aug 2020ListedStatusListed 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  • Withdrawn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
Delta Xtend
Generic Name
Total reverse shoulder prosthesis
Model / Ref / Catalog
1337-66-042, 133766042
Primary DI / UDI-DI
10603295523161
510(k) Number
FDA Product Code
HSD, PHX, KWS
GMDN Term
Total reverse shoulder prosthesis
Device Class
Class II
Regulation Number
888.3690, 888.3660
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Total reverse shoulder prosthesis

Cleared under the same submission (K183077)

Show all (12)

Other devices from Depuy (Ireland)

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Properties

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

Other properties (8)

  • 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