CAPRI™ Corpectomy Cage System

FDA UDI

Class II (US FDA UDI)

by K2m, Inc.

Identity

Trade Name: CAPRI™ Corpectomy Cage System FDA UDI
Generic Name: Vertebral body prosthesis FDA UDI
Device Name: Solid Corpectomy Cage, Size 13x16x24 mm, 7° FDA UDI
Model / Reference: 7501-21624L7-G2 FDA UDI
Description: Solid Corpectomy Cage, Size 13x16x24 mm, 7° FDA UDI

Identifiers

Catalog Number: 7501-21624L7-G2 FDA UDI
Primary DI / UDI-DI: 10888857333130 FDA UDI
FDA Product Code: MQP FDA UDI
PLR FDA UDI
GMDN Term: Vertebral body prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 13 Millimeter FDA UDI
Height — 24 Millimeter FDA UDI
Width — 16 Millimeter FDA UDI
Angle — 7 degree FDA UDI

Category: Vertebral body prosthesis

CAPRI™ Corpectomy Cage System by K2m, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral body prosthesis.

FORTIFY — GLOBUS MEDICAL, INC. · Class II
VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
Novel — ALPHATEC SPINE, INC. · Class II
Regatta — SeaSpine Orthopedics Corporation · Class II
C-THRU™ Anterior Spinal System — BIOMET SPINE LLC · Class II
VERTE-STACK® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
Novel — ALPHATEC SPINE, INC. · Class II
XPAND-R — GLOBUS MEDICAL, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: K2m, Inc.

Sources (1)

FDA UDI f8a7449a-2637-4f9b-bdfa-9a2c9f2ac8ea 36 fields · synced Jun 1, 2026