← Back to catalogue

The JASPER Spinal Fixation System

FDA UDI

Class II (US FDA UDI)

by GBS Commonwealth Co., Ltd.

Identity

Trade Name
The JASPER Spinal Fixation System FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Model / Reference
L11A-75130 FDA UDI

Identifiers

Primary DI / UDI-DI
08800057223894 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system, non-sterile

The JASPER Spinal Fixation System by GBS Commonwealth Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-screw internal spinal fixation system, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7a6d6c51-a35d-4946-a5c1-68125835391b 33 fields · synced May 30, 2026