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Stature®

FDA UDI

Class II (US FDA UDI)

by Atlas Spine Inc.

Identity

Trade Name
Stature® FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
11mm Non-Lordotic Spacer FDA UDI
Model / Reference
STF-011-008 FDA UDI
Description
11mm Non-Lordotic Spacer FDA UDI

Identifiers

Catalog Number
STF-011-008 FDA UDI
Primary DI / UDI-DI
M681STF0110080 FDA UDI
FDA Product Code
MQP FDA UDI
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 FDA UDI
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 11 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Stature® by Atlas Spine Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atlas Spine Inc.

Sources (1)

  • FDA UDI d48f1e1f-a14b-4649-a1c0-ec312fc309b2 35 fields · synced May 31, 2026