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Ascend

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
Ascend FDA UDI
Generic Name
Vertebral body prosthesis FDA UDI
Device Name
16mm CORE EXP, 26-36mm FDA UDI
Model / Reference
157-0-16-26 FDA UDI
Description
16mm CORE EXP, 26-36mm FDA UDI

Identifiers

Primary DI / UDI-DI
00190376632711 FDA UDI
510(k) Number
K232173 FDA UDI
FDA Product Code
MQP FDA UDI
PLR FDA UDI
GMDN Term
Vertebral body prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3060 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 36 Millimeter FDA UDI
Height — 26 Millimeter FDA UDI

Category: Vertebral body prosthesis

Ascend by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vertebral body prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8b0fe61d-bac5-495d-9e48-5e9b2a7cd149 36 fields · synced Jun 8, 2026