LOSPA IS Spinal System
- Primary DI
- 08806373837135
- Brand
- LOSPA IS Spinal System
- Company
- Corentec Co., Ltd
- Model
- 01.22.922
- Device description
- Rod Link(B Type)
- Published
- 2015-10-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K092076 | 000 | AEGIS & AEGIS II SPINAL SYSTEM | Corentec Co., Ltd. | 2010-04-02 | MNI |
| K132644 | 000 | LOSPA IS PEDICLE SCREW (MONOAXIAL & POLYAXIAL), LOSPA IS ROD- STRAIGHT (STANDARD), LOSPA IS ROD- PRE BENT (STANDARD & BU | Corentec Co., Ltd. | 2013-09-19 | MNI |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08806373837135 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08806373837135 | 08806373837135 | 8806373837135 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone-screw internal spinal fixation system connector | An implantable component of a bone-screw internal spinal fixation system typically in the form of a thin band or small rod with a groove or hole at each end, into which screw heads/rods fit, intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is designed as a transverse connecting element to be attached to corresponding bilateral screw heads or rods; it may also have adjustable length and/or angle and/or allow a small amount of screw/rod movement. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +82269374902 | ra@corentec.com |
Regulatory Flags#
- DUNS number
- 688739895
- Device count
- 1
- Lot or batch
- true
- Manufacturing date on label
- true
- Sterilization required before use
- true
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| 08800017261478 | EXULT Knee Replacement System | K3.IAN.4572-11T | 2020-01-10 |
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