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Zavation

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Balloon kyphoplasty kit FDA UDI
Device Name
8 Gauge 20mm Traditional Single Kyphoplasty Balloon Kit FDA UDI
Model / Reference
VCF-0820-TDK FDA UDI
Description
8 Gauge 20mm Traditional Single Kyphoplasty Balloon Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00197157005832 FDA UDI
510(k) Number
K141419 FDA UDI
FDA Product Code
NDN FDA UDI
HRX FDA UDI
GAA FDA UDI
GMDN Term
Balloon kyphoplasty kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3027 FDA UDI
888.1100 FDA UDI
878.4800 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

No

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
Ethylene Oxide FDA UDI

Category: Balloon kyphoplasty kit

Zavation by Zavation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Balloon kyphoplasty kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zavation

Sources (1)

  • FDA UDI 7769b8af-ea15-4e77-b4aa-f38e694816f3 35 fields · synced May 30, 2026