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BLACKHAWK Cervical Spacer System

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
BLACKHAWK Cervical Spacer System FDA UDI
Generic Name
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
BLACKHAWK TI,INSERTER,MAIN CORE V2 FDA UDI
Model / Reference
T070-0001-A3 FDA UDI
Description
BLACKHAWK TI,INSERTER,MAIN CORE V2 FDA UDI

Identifiers

Primary DI / UDI-DI
00840996192408 FDA UDI
510(k) Number
K171489 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical implant/trial-implant/sizer holder, reusable 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: Surgical implant/trial-implant/sizer holder, reusable

BLACKHAWK Cervical Spacer System by Choicespine, LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant/trial-implant/sizer holder, reusable.

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 73ed53e0-6677-4ab7-a21e-6ca7fe0c665d 34 fields · synced Jun 1, 2026