DELTA XTEND
- Primary DI
- 10603295027249
- Brand
- DELTA XTEND
- Company
- DEPUY (IRELAND)
- Model
- 130714110
- Catalog number
- 130714110
- Device description
- DELTA Xtend Monobloc Hum Cemented Epiphysis Sz1 /Dia14 LG
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K062250 | 000 | DELTA XTEND REVERSE SHOULDER SYSTEM | DePuy Orthopaedics, Inc. | 2007-02-02 | PHX |
| K120174 | 000 | DEPUT DELTA XTEND REVERSE SHOULDER | Depuy France | 2012-06-11 | PHX |
| K192855 | 000 | DELTA XTEND(TM) Reverse Shoulder System | Depuy(Ireland) | 2020-02-24 | PHX |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10603295027249 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10603295027249 | 10603295027249 |
GMDN Terms#
| Term | Definition |
|---|---|
| Total reverse shoulder prosthesis | A sterile implantable artificial substitute for a shoulder joint designed to replace both articulating surfaces of the joint particularly in patients with chronic, longstanding rotator cuff muscle tears, arthritis, and/or humeral fractures unsuccessfully treated by previous surgery. The device reverses normal anatomy so that the head portion of the joint is attached to the scapula and the socket portion is attached to the humerus. It typically includes a humeral stem and glenosphere (head) with body and cup components. The device may include screws for implantation and may be implanted with or without bone cement. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 989365556
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10603295079941 | AML EXCEL | 2001-42-000 | 200142000 | 2018-09-24 |
| 10603295080008 | AML EXCEL | 2001-47-000 | 200147000 | 2018-09-24 |
| 10603295080015 | AML EXCEL | 2001-48-000 | 200148000 | 2018-09-24 |
| 10603295080022 | AML EXCEL | 2001-49-000 | 200149000 | 2018-09-24 |
| 10603295080145 | NA | 2001-80-501 | 200180501 | 2018-09-24 |
| 10603295080770 | NA | 2002-25-000 | 200225000 | 2018-09-24 |
| 10603295080787 | NA | 2002-27-000 | 200227000 | 2018-09-24 |
| 10603295080794 | NA | 2002-31-000 | 200231000 | 2018-09-24 |
| 10603295082057 | TRI-LOCK | 2012-03-005 | 201203005 | 2018-09-24 |
| 10603295082064 | TRI-LOCK | 2012-03-010 | 201203010 | 2018-09-24 |
| 10603295082071 | TRI-LOCK | 2012-03-020 | 201203020 | 2018-09-24 |
| 10603295082088 | TRI-LOCK | 2012-03-030 | 201203030 | 2018-09-24 |
| 10603295082095 | TRI-LOCK | 2012-03-040 | 201203040 | 2018-09-24 |
| 10603295082101 | TRI-LOCK | 2012-03-050 | 201203050 | 2018-09-24 |
| 10603295082118 | TRI-LOCK | 2012-03-060 | 201203060 | 2018-09-24 |
| 10603295082125 | TRI-LOCK | 2012-03-070 | 201203070 | 2018-09-24 |
| 10603295082132 | TRI-LOCK | 2012-03-080 | 201203080 | 2018-09-24 |
| 10603295082149 | TRI-LOCK | 2012-03-090 | 201203090 | 2018-09-24 |
| 10603295082156 | TRI-LOCK | 2012-03-100 | 201203100 | 2018-09-24 |
| 10603295082163 | TRI-LOCK | 2012-03-110 | 201203110 | 2018-09-24 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| B1132A2HI000100 | Shoulder Innovations InSet 95 Humeral Stem | Shoulder Innovations, Inc. | KWS | 2026-05-28 |
| B1132A2HI000100 | Shoulder Innovations InSet 95 Humeral Stem | Shoulder Innovations, Inc. | HSD | 2026-05-28 |
| 07613327354331 | REUNION | Stryker GmbH | KWS | 2022-11-15 |
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| 07613327355246 | REUNION | Stryker GmbH | KWS | 2022-11-15 |