Pyramesh® Implant System
- Primary DI
- 00763000856632
- Brand
- Pyramesh® Implant System
- Company
- MEDTRONIC SOFAMOR DANEK, INC.
- Model
- 905-903
- Device description
- MESH 905-903 PYRM 19 X 150 ANGLED
- Published
- 2025-07-18
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00763000856632 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00763000856632 | 00763000856632 | 763000856632 | 0763000856632 |
GMDN Terms#
| Term | Definition |
|---|---|
| Extra-gynaecological surgical mesh, metal | A non-bioabsorbable, implantable material (e.g., flat sheet) made from made from a biocompatible metal, with appropriate mechanical characteristics for implantation, intended for an extra-gynaecological tissue repair/reinforcement application(s) to support or protect tissues in reconstructive surgical procedures (e.g., to repair large chest wall defects or large abdominal incisional hernias) and/or orthopaedic procedures (e.g., cranioplasty, femoral reconstruction); it is not primarily intended for dental use. Disposable devices associated with implantation may be supplied with the mesh. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 830350380
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00643169236967 | n/a | 7480653 | 2026-10-11 | |
| 00643169236974 | n/a | 7480652 | 2026-10-11 | |
| 00643169236981 | n/a | 7480651 | 2026-10-11 | |
| 00763000857851 | T2 STRATOSPHERE™ Expandable Corpectomy System | 4361258 | 2026-10-11 | |
| 00763000857950 | T2 STRATOSPHERE™ Expandable Corpectomy System | 4361225 | 2026-10-11 | |
| 00763000874209 | MSB SHILLA Growth Guidance System | 7674500 | 2026-10-11 | |
| 00763000885502 | MSB Reusable Instruments | 7080921D | 2026-10-11 | |
| 00824846010722 | Medtronic Reusable Instruments | X0726002 | 2026-10-09 | |
| 00643169964938 | GRAFTON™ DBM | T42275INT | 2024-12-05 | |
| 00643169965102 | GRAFTON PLUS™ DBM | T45005INT | 2024-11-15 | |
| 00763000140502 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 000505 | 2021-03-12 | |
| 00763000140519 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 005001 | 2021-03-12 | |
| 00763000140526 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 005005 | 2021-03-12 | |
| 00763000140533 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 005110 | 2021-03-12 | |
| 00763000140540 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 006001 | 2021-03-12 | |
| 00763000140557 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 006002 | 2021-03-12 | |
| 00763000140564 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 006005 | 2021-03-12 | |
| 00763000140571 | PROGENIX™ PUTTY and PROGENIX™ PLUS | 006010 | 2021-03-12 | |
| 00643169965089 | GRAFTON® DBM | T44150INT | 2019-02-07 | |
| 00613994247612 | PROGENIX® PUTTY and PROGENIX® PLUS | 005110 | 2019-03-29 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00763000857851 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-10-11 |
| 00763000857950 | T2 STRATOSPHERE™ Expandable Corpectomy System | MEDTRONIC SOFAMOR DANEK, INC. | MQP | 2026-10-11 |
| 10888857160460 | CASCADIA™ Interbody System | VB Spine LLC | MQP | 2018-04-16 |
| 10888857223769 | CASCADIA™ Interbody System | VB Spine LLC | MQP | 2018-02-08 |
| 10888857223776 | CASCADIA™ Interbody System | VB Spine LLC | MQP | 2018-02-08 |
| 10888857223783 | CASCADIA™ Interbody System | VB Spine LLC | MQP | 2018-02-08 |
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