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AVATAR Minimally Invasive Spinal System

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name
AVATAR Minimally Invasive Spinal System FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
Retaining Nut for Compression Distraction Plate FDA UDI
Model / Reference
2013-0066 FDA UDI
Description
Retaining Nut for Compression Distraction Plate FDA UDI

Identifiers

Catalog Number
2013-0066 FDA UDI
Primary DI / UDI-DI
00190837055349 FDA UDI
510(k) Number
K111953 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal bone screw, non-bioabsorbable

AVATAR Minimally Invasive Spinal System by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Spine, Inc.

Sources (1)

  • FDA UDI 8c7d7c6d-7ca8-4ace-a46e-da941ad1d6a4 35 fields · synced Jun 6, 2026