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EquiLOX Lumbar Expandable Cage

FDA UDI

Class II (US FDA UDI)

by Captiva Spine

Identity

Trade Name
EquiLOX Lumbar Expandable Cage FDA UDI
Generic Name
Spinal fusion sphere FDA UDI
Device Name
Expandable Lumbar Cage 24mm (L) x 10mm (W) x 9mm (H1) - 14mm (H2) x 6deg (LA) FDA UDI
Model / Reference
CSF0301-B0024A956S FDA UDI
Description
Expandable Lumbar Cage 24mm (L) x 10mm (W) x 9mm (H1) - 14mm (H2) x 6deg (LA) FDA UDI

Identifiers

Primary DI / UDI-DI
00850065741093 FDA UDI
510(k) Number
K232069 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Spinal fusion sphere 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

Yes

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

Category: Spinal fusion sphere

EquiLOX Lumbar Expandable Cage by Captiva Spine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fusion sphere.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Captiva Spine

Sources (1)

  • FDA UDI 75a8ccce-7501-468d-b2d5-29120a788e11 35 fields · synced May 30, 2026