← Back to catalogue

Thunderbolt

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
THUNDERBOLT FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
THUNDERBOLT,JAMSHIDI GUIDE FDA UDI
Model / Reference
M070-0200 FDA UDI
Description
THUNDERBOLT,JAMSHIDI GUIDE FDA UDI

Identifiers

Primary DI / UDI-DI
00840996192576 FDA UDI
510(k) Number
K171456 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone-screw internal spinal fixation system, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Thunderbolt by Choicespine, LP — Class I — 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

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI ed70ca02-ace1-4503-8ed8-5795c351d046 34 fields · synced May 29, 2026