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Zavation

FDA UDI

Class II (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Bone matrix implant, animal-derived, bioabsorbable FDA UDI
Device Name
ZV Graft FDA UDI
Model / Reference
02-030-03-ZVG FDA UDI
Description
ZV Graft FDA UDI

Identifiers

Primary DI / UDI-DI
00842166115484 FDA UDI
510(k) Number
K102937 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, animal-derived, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Bone matrix implant, animal-derived, bioabsorbable

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

Similar devices

Also classified as Bone matrix implant, animal-derived, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zavation

Sources (1)

  • FDA UDI fb9e231d-aa79-4e8d-877b-835f1209b964 35 fields · synced Jun 6, 2026