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Zavation

FDA UDI

Class I (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Balloon kyphoplasty kit FDA UDI
Device Name
ZVplasty System Assembly FDA UDI
Model / Reference
VCF-1015-1G-E FDA UDI
Description
ZVplasty System Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
00842166126725 FDA UDI
510(k) Number
K141419 FDA UDI
FDA Product Code
GAA FDA UDI
HRX FDA UDI
NDN FDA UDI
GMDN Term
Balloon kyphoplasty kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
888.1100 FDA UDI
888.3027 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Balloon kyphoplasty kit

Zavation by Zavation — Class I — 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 ea78da5f-9d05-4788-8455-61b49d4dca10 35 fields · synced Jun 1, 2026