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STARFIRE™ Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
STARFIRE™ Pedicle Screw System FDA UDI
Generic Name
Bone-screw internal spinal fixation system, non-sterile FDA UDI
Device Name
STARFIRE,HANDLE,TULIP POSITIONER FDA UDI
Model / Reference
E070-0046 FDA UDI
Description
STARFIRE,HANDLE,TULIP POSITIONER FDA UDI

Identifiers

Primary DI / UDI-DI
00840996125420 FDA UDI
510(k) Number
K102204 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

STARFIRE™ Pedicle Screw System 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

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Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI fa3a7a5c-43e8-4729-ab3c-908c6c8bbfbb 35 fields · synced May 31, 2026