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Lancer Open Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
Lancer Open Pedicle Screw System FDA UDI
Generic Name
External spinal fixation system FDA UDI
Device Name
Tapered Cannulated T25 Driver FDA UDI
Model / Reference
M070-0133 FDA UDI
Description
Tapered Cannulated T25 Driver FDA UDI

Identifiers

Primary DI / UDI-DI
00840996177382 FDA UDI
FDA Product Code
LHX FDA UDI
GMDN Term
External spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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: External spinal fixation system

Lancer Open Pedicle Screw System by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External spinal fixation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI b367192a-e949-4227-9bd9-cea370d0769c 34 fields · synced Jun 8, 2026