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CAPRI™ Corpectomy Cage System

FDA UDI

Class I (US FDA UDI)

by K2m, Inc.

Identity

Trade Name
CAPRI™ Corpectomy Cage System FDA UDI
Generic Name
Internal spinal fixation procedure kit, single-use FDA UDI
Device Name
Malleable Retractor, Size 50 mm FDA UDI
Model / Reference
8101-90015 FDA UDI
Description
Malleable Retractor, Size 50 mm FDA UDI

Identifiers

Catalog Number
8101-90015 FDA UDI
Primary DI / UDI-DI
10888857347199 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Internal spinal fixation procedure kit, single-use 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

Yes

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

Yes

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: Internal spinal fixation procedure kit, single-use

A comprehensive orthopedic manual surgical instrument used for internal spinal fixation and fusion cage implantation procedures. Learn about its key features, regulatory compliance, and more.

Similar devices

Also classified as Internal spinal fixation procedure kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
K2m, Inc.

Sources (1)

  • FDA UDI 5d0f2f75-442d-4f3b-ba35-f68082cd2088 35 fields · synced Jul 27, 2026