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MacroFORM MIS Composite 2.5cc

FDA UDI

Class II (US FDA UDI)

by NovaBone Products, LLC

Identity

Trade Name
MacroFORM MIS Composite 2.5cc FDA UDI
Generic Name
Bone matrix implant, composite FDA UDI
Device Name
Synthetic bone void filler for orthopedic applications FDA UDI
Model / Reference
NB4400 FDA UDI
Description
Synthetic bone void filler for orthopedic applications FDA UDI

Identifiers

Catalog Number
NB4400 FDA UDI
Primary DI / UDI-DI
00813909011493 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, composite 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, composite

MacroFORM MIS Composite 2.5cc by NovaBone Products, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, composite.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f756444c-033a-439f-80d0-a9a3a31f6674 36 fields · synced Jun 9, 2026