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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
Reverse shoulder prosthesis head FDA UDI
Device Name
DELTA XTEND Lateralized Glenosphere +2mm Eccentric 038mm FDA UDI
Model / Reference
1307-62-038 FDA UDI
Description
DELTA XTEND Lateralized Glenosphere +2mm Eccentric 038mm FDA UDI

Identifiers

Catalog Number
130762038 FDA UDI
Primary DI / UDI-DI
10603295502432 FDA UDI
510(k) Number
K183077 FDA UDI
K192855 FDA UDI
FDA Product Code
KWS FDA UDI
PHX FDA UDI
HSD FDA UDI
GMDN Term
Reverse shoulder prosthesis head FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 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: Reverse shoulder prosthesis head

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

Similar devices

Also classified as Reverse shoulder prosthesis head.

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 14c4dd70-6bbb-4279-80a5-5823a9fd8413 36 fields · synced May 30, 2026