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Harrier SA

FDA UDI

Class II (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
Harrier SA FDA UDI
Generic Name
Intervertebral-body internal spinal fixation system FDA UDI
Device Name
Harrier SA 26x32x8, 10 Deg FDA UDI
Model / Reference
Y070-26321008 FDA UDI
Description
Harrier SA 26x32x8, 10 Deg FDA UDI

Identifiers

Primary DI / UDI-DI
00840996177245 FDA UDI
510(k) Number
K180519 FDA UDI
FDA Product Code
MAX FDA UDI
OVD FDA UDI
GMDN Term
Intervertebral-body internal spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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: Intervertebral-body internal spinal fixation system

Harrier SA by Choicespine, LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intervertebral-body internal spinal fixation system.

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 d3ee0ad4-626c-48fc-9500-3fd8f51e2e3e 35 fields · synced May 31, 2026