LOSPA IS Spinal System
- Primary DI
- 08806373870477
- Brand
- LOSPA IS Spinal System
- Company
- Corentec Co., Ltd
- Model
- SI.C50.0016
- Device description
- PLIF HOLDER CURVED OUS TYPE
- Published
- 2018-02-21
- Public version status
- Update
- Distribution status
- 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 |
|---|---|
| K151408 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08806373870477 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08806373870477 | 08806373870477 | 8806373870477 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic implant/trial-implant/sizer holder, reusable | A hand-held manual surgical instrument designed to connect to and hold an orthopaedic implant (e.g., bone screw, bone graft), trial implant, or sizer (e.g., glenoid defect sizer) to facilitate guidance, gauging/sizing, and/or monitoring of the held device during an orthopaedic surgical intervention. The instrument is typically made of high-grade stainless steel or synthetic polymer materials and is typically constructed in the form of a long shaft with a handle at the proximal end and a device holding/fixation mechanism at the distal end (e.g., a threaded portion or a clamp mechanism). This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +820415857114 | hckoh@corentec.com |
Regulatory Flags#
- DUNS number
- 688739895
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 08800068946966 | BENCOX | HA.018.2835 | 2026-07-01 | |
| 08800068946973 | BENCOX | HA.018.4062 | 2026-07-01 | |
| 08800068963666 | BENCOX | HA.018.3642 | 2026-07-01 | |
| 08806373897344 | BENCOX | HA.018.2837 | 2026-07-01 | |
| 08806373897351 | BENCOX | HA.018.3239 | 2026-07-01 | |
| 08806373897368 | BENCOX | HA.018.3644 | 2026-07-01 | |
| 08806373897375 | BENCOX | HA.018.3648 | 2026-07-01 | |
| 08806373897382 | BENCOX | HA.018.3652 | 2026-07-01 | |
| 08809945870332 | BENCOX Instrument | HA.014.0004 | 2024-04-24 | |
| 08800068983558 | BENCOX | HA.0B8.0001 | 2026-07-24 | |
| 08800017271095 | BENCOX | HA.02G.0001 | 2026-04-10 | |
| 08800017269726 | EXULT Knee Replacement System | K3.FAL.7376 | 2020-05-21 | |
| 08800017269733 | EXULT Knee Replacement System | K3.FAR.7376 | 2020-05-21 | |
| 08800017269740 | EXULT Knee Replacement System | K3.FAL.7678 | 2020-05-21 | |
| 08800017269757 | EXULT Knee Replacement System | K3.FAR.7678 | 2020-05-21 | |
| 08800017269764 | EXULT Knee Replacement System | K3.FBL.7376 | 2020-05-21 | |
| 08800017269771 | EXULT Knee Replacement System | K3.FBR.7376 | 2020-05-21 | |
| 08800017269788 | EXULT Knee Replacement System | K3.FBL.7678 | 2020-05-21 | |
| 08800017269795 | EXULT Knee Replacement System | K3.FBR.7678 | 2020-05-21 | |
| 08800017260853 | EXULT Knee Replacement System | K3.BFN.3657 | 2020-01-10 |
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| B707125355730600 | DUALX DUAL PORTAL DISPOSABLE KIT-60MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
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| B707125355730900 | DUALX DUAL PORTAL DISPOSABLE KIT-90MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355731000 | DUALX DUAL PORTAL DISPOSABLE KIT-100MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
| B707125355731100 | DUALX DUAL PORTAL DISPOSABLE KIT-110MM (USA) | AMPLIFY SURGICAL, INC. | MAX | 2026-09-04 |
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