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AttraX

FDA UDI

Class II (US FDA UDI)

by Nuvasive, Inc.

Identity

Trade Name
AttraX FDA UDI
Generic Name
Bone matrix implant, synthetic, non-antimicrobial FDA UDI
Device Name
AttraX® Scaffold Morsels, 30cc FDA UDI
Model / Reference
5015130 FDA UDI
Description
AttraX® Scaffold Morsels, 30cc FDA UDI

Identifiers

Primary DI / UDI-DI
00887517939975 FDA UDI
510(k) Number
K090641 FDA UDI
K151584 FDA UDI
K172497 FDA UDI
K191974 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, synthetic, non-antimicrobial 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

Yes

FDA UDI

Category: Bone matrix implant, synthetic, non-antimicrobial

AttraX by Nuvasive, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, synthetic, non-antimicrobial.

Cleared under the same submission

K090641 also covers:

K151584 also covers:

K172497 also covers:

K191974 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nuvasive, Inc.

Sources (1)

  • FDA UDI 4d381c43-aee8-45e3-90f8-ca3403c124d5 35 fields · synced May 30, 2026