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HAWKEYE Vertebral Body Replacement (VBR)

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
HAWKEYE Vertebral Body Replacement (VBR) FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
HAWKEYE,Ti,SPACER,14X16X54, 0DEG FDA UDI
Model / Reference
WT10-14160054 FDA UDI
Description
HAWKEYE,Ti,SPACER,14X16X54, 0DEG FDA UDI

Identifiers

Primary DI / UDI-DI
00840996163590 FDA UDI
510(k) Number
K171686 FDA UDI
FDA Product Code
MQP FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI
Height — 54 Millimeter FDA UDI
Width — 14 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

HAWKEYE Vertebral Body Replacement (VBR) by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

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 4cfe6006-5ff5-442a-b425-505e6edfa3b7 36 fields · synced Jun 6, 2026