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Squadron Lumbar Cage

FDA UDI

Class II (US FDA UDI)

by Valorus Spine, Llc

Identity

Trade Name
Squadron Lumbar Cage FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
Squadron Parallel Bullet Nose PLIF Cage, 28mm x 9mm x 7mm FDA UDI
Model / Reference
31-01-280907 FDA UDI
Description
Squadron Parallel Bullet Nose PLIF Cage, 28mm x 9mm x 7mm FDA UDI

Identifiers

Primary DI / UDI-DI
00811771035845 FDA UDI
510(k) Number
K171914 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage 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

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

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: Polymeric spinal interbody fusion cage

Squadron Lumbar Cage by Valorus Spine, Llc — 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
Valorus Spine, Llc

Sources (1)

  • FDA UDI 3865defa-8de3-42f9-b6cb-a3127f287db6 35 fields · synced Jun 8, 2026