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Lateral Patient Positioning System

FDA UDI

Class I (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
Lateral Patient Positioning System FDA UDI
Generic Name
Spinal surgery positioning board FDA UDI
Device Name
Loading Base A FDA UDI
Model / Reference
181-600-1 FDA UDI
Description
Loading Base A FDA UDI

Identifiers

Primary DI / UDI-DI
00190376484259 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Spinal surgery positioning board FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spinal surgery positioning board

Lateral Patient Positioning System by Alphatec Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal surgery positioning board.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 346f6711-7545-4837-ae9e-a57863efae27 34 fields · synced Jun 8, 2026