TiWedge™
- Primary DI
- 10381780237686
- Brand
- TiWedge™
- Company
- Ascension Orthopedics, Inc.
- Model
- TRL-1006-C06
- Device description
- The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended to be used for angular correction of small bones in the ankle and foot. The Integra Titanium Bone Wedges are constructed from commercially pure titanium formed into a cancellous-like structure. Trial Cotton 20 X 6.5
- Published
- 2016-08-08
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K131360 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10381780237686 | Primary | GS1 | 0 | |
| M269TRL1006C061 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780237686 | 10381780237686 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)654-2873 | custsvcnj@integralife.com |
Regulatory Flags#
- DUNS number
- 942377524
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 10381780240204 | Cadence™ | 10203022 | 2016-08-24 | |
| 10381780240211 | Cadence™ | 10203023 | 10203023 | 2016-08-24 |
| 10381780240228 | Cadence™ | 10203024 | 10203024 | 2016-08-24 |
| 10381780240235 | Cadence™ | 10203025 | 2016-08-24 | |
| 10381780240242 | Cadence™ | 10203026 | 2016-08-24 | |
| 10381780240754 | Cadence™ | 10204202 | 10204202 | 2016-08-24 |
| 10381780245612 | Titan™ | IMC096004301 | IMC-0960-043-01 | 2017-08-30 |
| 10381780246374 | Integra® | OSG20000 | OSG-200-00 | 2017-08-30 |
| 10381780246381 | Integra® | OSG20010P | OSG-200-10P | 2017-08-30 |
| 10381780246398 | Integra® | OSG20010PV | OSG-200-10PV | 2017-08-30 |
| 10381780246404 | Integra® | OSG20020P | OSG-200-20P | 2017-08-30 |
| 10381780246411 | Integra® | OSG20020PV | OSG-200-20PV | 2017-08-30 |
| 10381780246428 | Integra® | OSG20030P | OSG-200-30P | 2017-08-30 |
| 10381780246435 | Integra® | OSG20030PV | OSG-200-30PV | 2017-09-05 |
| 10381780246442 | Integra® | OSG20040P | OSG-200-40P | 2017-09-05 |
| 10381780246459 | Integra® | OSG20040PV | OSG-200-40PV | 2017-08-30 |
| 10381780246466 | Integra® | OSG35001 | OSG-350-01 | 2017-08-30 |
| 10381780246473 | Integra® | OSG44200 | OSG-442-00 | 2017-09-05 |
| 10381780246480 | First Choice® DRUJ System | OSG60000 | OSG-600-00 | 2017-09-05 |
| 10381780246497 | First Choice® DRUJ System | OSG60001 | OSG-600-01 | 2017-09-05 |
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