Titan™ Reverse Shoulder System
- Primary DI
- 10381780121534
- Brand
- Titan™ Reverse Shoulder System
- Company
- Ascension Orthopedics, Inc.
- Model
- BBS096021STD
- Catalog number
- BBS-0960-21STD
- Device description
- The Titan Reverse Shoulder humeral body is made of titanium. It is designed for potential increased ROM and minimized scapular notching, as well as increased visual and access to glenoid. The asymmatrix coating allows for an all press fit humeral component and secondary fixation. A titanium screw is included for fixation.
- Published
- 2017-10-09
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWS | Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K130050 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10381780121534 | Primary | GS1 | 0 | |
| M269BBS096021STD1 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780121534 | 10381780121534 |
GMDN Terms#
| Term | Definition |
|---|---|
| Reverse shoulder prosthesis body | A sterile component of a reverse shoulder prosthesis that consists of a metallic piece [e.g., cobalt-chrome-molybdenum (Co-Cr-Mo)], which may be coated [e.g., with hydroxyapatite (HA)], intended to form a connection between a humeral stem prosthesis and a reverse shoulder prosthesis cup. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Contacts#
| Phone | |
|---|---|
| +1(800)654-2873 | custsvcnj@integralife.com |
Regulatory Flags#
- DUNS number
- 942377524
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 10381780240310 | Cadence™ | 10203193 | 2016-08-24 | |
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| 10381780245629 | Titan™ | IP0920055001 | IMP-0920-055-001 | 2017-09-05 |
| 10381780245636 | Titan™ | IP0920064001 | IMP-0920-064-001 | 2017-09-05 |
| 10381780245643 | Titan™ | IP0920079501 | IMP-0920-0795-01 | 2017-09-05 |
| 10381780245650 | Titan™ | IMP096006401 | IMP-0960-064-01 | 2017-09-05 |
| 10381780245667 | Titan™ | IMP096006601 | IMP-0960-066-01 | 2017-09-05 |
| 10381780245674 | Titan™ | IMP096007101 | IMP-0960-071-01 | 2017-09-05 |
| 10381780245681 | Ascension® | IMP10000D | IMP-100-00D | 2017-09-05 |
| 10381780245698 | Ascension® | IMP10000P | IMP-100-00P | 2017-09-05 |
| 10381780245704 | Integra® | IMP20000D | IMP-200-00D | 2017-09-05 |
| 10381780245711 | Integra® | IMP20000P | IMP-200-00P | 2017-09-05 |
| 10381780245728 | Integra® | IMP30000 | IMP-300-00 | 2017-09-05 |
| 10381780245735 | Integra® | IMP35000 | IMP-350-00 | 2017-09-05 |
| 10381780245759 | NuGrip® CMC Implant System | IMP44200 | IMP-442-00 | 2017-09-05 |
| 10381780245766 | First Choice® DRUJ System | IMP60000 | IMP-600-00 | 2017-09-05 |
| 10381780245780 | Movement® | IMP-890-00MT | IMP-890-00MT | 2017-09-05 |
| 10381780245797 | Movement® | IMP-890-00PP | IMP-890-00PP | 2017-09-05 |
| 10381780245803 | Integra® | IMP90001 | IMP-900-01 | 2017-09-05 |
| 10381780245988 | Integra® | MAL092008501 | MAL-0920-085-01 | 2017-08-30 |
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|---|---|---|---|---|
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