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Delta Xtend

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
DELTA XTEND FDA UDI
Generic Name
Total reverse shoulder prosthesis FDA UDI
Device Name
DELTA XTEND Modular 155 Degree Epiphysis POROCOAT SIZE 2 - RIGHT FDA UDI
Model / Reference
1307-30-203 FDA UDI
Description
DELTA XTEND Modular 155 Degree Epiphysis POROCOAT SIZE 2 - RIGHT FDA UDI

Identifiers

Catalog Number
130730203 FDA UDI
Primary DI / UDI-DI
10603295510314 FDA UDI
510(k) Number
K192855 FDA UDI
FDA Product Code
PHX FDA UDI
KWS FDA UDI
GMDN Term
Total reverse shoulder prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Total reverse shoulder prosthesis

Delta Xtend by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total reverse shoulder prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI 1abd41a8-2ed9-46ef-9d1c-26c28df02697 36 fields · synced May 30, 2026