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ClariVy™

FDA UDI

Class II (US FDA UDI)

by Vy Spine Llc

Identity

Trade Name
ClariVy™ FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
IBF, Sterile, 14x11, 7°, 4mm, PEEK Optima LT1-HA FDA UDI
Model / Reference
02-C-1411-7-04-PH-R FDA UDI
Description
IBF, Sterile, 14x11, 7°, 4mm, PEEK Optima LT1-HA FDA UDI

Identifiers

Primary DI / UDI-DI
00840283400094 FDA UDI
510(k) Number
K212715 FDA UDI
FDA Product Code
OVE FDA UDI
ODP 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Polymeric spinal interbody fusion cage

ClariVy™ by Vy 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
Vy Spine Llc

Sources (1)

  • FDA UDI d5b15d66-c487-43dd-84b6-11c47971cf6a 35 fields · synced May 30, 2026