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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
Surgical implant/trial-implant/sizer holder, reusable FDA UDI
Device Name
Expandable Lumbar Cage 24mm (L) x 10mm (W) x 12mm (H1) - 17mm (H2) x 15deg (LA) FDA UDI
Model / Reference
CSF0301-B0024AC5FS FDA UDI
Description
Expandable Lumbar Cage 24mm (L) x 10mm (W) x 12mm (H1) - 17mm (H2) x 15deg (LA) FDA UDI

Identifiers

Primary DI / UDI-DI
00850065741123 FDA UDI
510(k) Number
K232069 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Surgical implant/trial-implant/sizer holder, reusable 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

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

Category: Surgical implant/trial-implant/sizer holder, reusable

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

Similar devices

Also classified as Surgical implant/trial-implant/sizer holder, reusable.

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 8fd12085-01b8-492d-8b0f-e48a596d207a 35 fields · synced Jun 6, 2026