Integra®
- Primary DI
- 10381780235002
- Brand
- Integra®
- Company
- Ascension Orthopedics, Inc.
- Model
- MRADHDINSTP
- Device description
- The Movement Great Toe System is used for hemi- and total-arthroplasty procedures. The hemi arthroplasty is intended for resurfacing of the 1st metatarsal head or the base of the proximal phalanx. The total arthroplasty is intended for resurfacing of the base of the 1st metatarso-phalangeal joint. This set includes metatarsal, proximal phalanx hemi, and proximal phalanx total trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials.
- Published
- 2016-08-15
- 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#
| Code | Name |
|---|---|
| KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWI | Prosthesis, Elbow, Hemi-, Radial, Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K032686 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10381780235002 | Primary | GS1 | 0 | |
| M268MRADHDINSTP1 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10381780235002 | 10381780235002 |
GMDN Terms#
| Term | Definition |
|---|---|
| General external orthopaedic fixation system implantation kit, reusable | A collection of mostly instruments intended to be used to manipulate and prepare soft-tissue and bone for the adjustment or placement of the implantable components of an external orthopaedic fixation system in various skeletal areas (e.g., bones of limbs, spine, pelvis, craniomaxillofacial areas). It is a non-dedicated device that includes various metallic and/or plastic reusable devices (e.g., retractors, rods, clamps, drills, pins, cutters, screwdrivers, guides, tighteners) that are specific to the fixation system applied; the implant(s) is not included. 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
- Kit
- true
- Serial number
- true
- Sterilization required before use
- 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 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 10886982300713 | NA | Synthes GmbH | KWI | 2020-06-17 |
| 10886982300720 | NA | Synthes GmbH | KWI | 2020-06-17 |
| 10886982300522 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300539 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300546 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300553 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300560 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300577 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300584 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300591 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300607 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300614 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300621 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300638 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300645 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300652 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300669 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300676 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300683 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300690 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300706 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300737 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300744 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300751 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300768 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300775 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300782 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300799 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300805 | NA | Synthes GmbH | KWI | 2020-06-08 |
| 10886982300812 | NA | Synthes GmbH | KWI | 2020-06-08 |