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Tiger Shark

FDA UDI

Class I (US FDA UDI)

by Choicespine, LP

Identity

Trade Name
Tiger Shark FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
Lumbar Interbody Rescue Tool, RW FDA UDI
Model / Reference
V070-1004R FDA UDI
Description
Lumbar Interbody Rescue Tool, RW FDA UDI

Identifiers

Primary DI / UDI-DI
00840996186278 FDA UDI
510(k) Number
K172816 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Metallic spinal interbody fusion cage 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

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: Metallic spinal interbody fusion cage

Tiger Shark by Choicespine, LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic 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 319f1024-8beb-4f53-a185-b88c900f27ee 34 fields · synced May 31, 2026