← Back to catalogue

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
TIGER SHARK,NERVE RETRACTOR,TALL DOUBLE FDA UDI
Model / Reference
P070-1015 FDA UDI
Description
TIGER SHARK,NERVE RETRACTOR,TALL DOUBLE FDA UDI

Identifiers

Primary DI / UDI-DI
00840996185684 FDA UDI
510(k) Number
K171456 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Choicespine, LP

Sources (1)

  • FDA UDI 770d6fdf-2843-46a6-8e2e-1fce74e2c159 34 fields · synced Jun 1, 2026