Identity
- Trade Name
- The JASPER Spinal Fixation System60 FDA UDI
- Generic Name
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
- Model / Reference
- L24G-80110 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800044754424 FDA UDI
- 510(k) Number
- K190762 FDA UDI
- FDA Product Code
- NKB FDA UDI
- GMDN Term
- Bone-screw internal spinal fixation system, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
Yes
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Bone-screw internal spinal fixation system, non-sterile
The JASPER Spinal Fixation System60 is a non-sterile, single-use orthopedic implant designed for the treatment of various spinal instabilities or deformities. As an internal spinal fixation system, it consists of a combination of anchors (e.g., bolts, hooks), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
Similar devices
Also classified as Bone-screw internal spinal fixation system, non-sterile.
- TIGER Spine System — CORELINK LLC · Class II
- SILVERTON SPINAL FIXATION SYSTEM — BIOMET SPINE LLC · Class II
- POLARIS™ 5.5 SPINAL SYSTEM — BIOMET SPINE LLC · Class II
- Vitality® — BIOMET SPINE LLC · Class II
- PASS LP — Medicrea International SA · Class II
- ALTA STAND-ALONE INTERBODY FUSION SYSTEM — BIOMET SPINE LLC · Class II
- ROMEO posterior osteosynthesis system — Spineart · Class II
- POLARIS 5.5 TI SPINAL SYSTEM — BIOMET SPINE LLC · Class II
Cleared under the same submission
K190762 also covers:
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
- The JASPER Spinal Fixation System — GBS Commonwealth Co., Ltd.
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- GBS Commonwealth Co., Ltd.
Sources (1)
- FDA UDI 6aa2f35b-ee5d-46eb-b23d-f82c8e5b53e8 33 fields · synced Jul 29, 2026