TITAN™
- Primary DI
- 10381780258698
- Brand
- TITAN™
- Company
- Ascension Orthopedics, Inc.
- Model
- GLN-0926-030-02A
- Device description
- The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg that is used in patients with severely painful and/or disabled joint, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The glenoid component is intended for cemented use only.
- Published
- 2016-05-19
- 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 |
|---|---|
| K152047 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10381780258698 | Primary | GS1 | 0 | |
| M269GLN092603002A1 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780258698 | 10381780258698 |
GMDN Terms#
| Term | Definition |
|---|---|
| Shoulder glenoid fossa prosthesis, prefabricated | An implantable, prefabricated component of a total shoulder prosthesis (glenoid component) designed to replace or repair the glenoid fossa; it is not a custom-made device. It is cup-like in shape and typically made of polyethylene (PE), but may be made of metal or a combination of PE and metal; it may include fixation devices (e.g., screws) for attachment to the scapula. |
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#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10381780240310 | Cadence™ | 10203193 | 2016-08-24 | |
| 10381780245513 | BioMotion® Cannulated 1st MPJ Hemi System | HM 3010 | HM 3010 | 2017-09-05 |
| 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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