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Alamo P, Alamo T

FDA UDI

Class I (US FDA UDI)

by Alliance Partners Llc

Identity

Trade Name
Alamo P, Alamo T FDA UDI
Generic Name
Orthopaedic surgical distractor, internal FDA UDI
Device Name
Paddle Starter Instrument FDA UDI
Model / Reference
2100T-1501 FDA UDI
Description
Paddle Starter Instrument FDA UDI

Identifiers

Catalog Number
2100T-1501 FDA UDI
Primary DI / UDI-DI
M6862100T15010 FDA UDI
510(k) Number
K120401 FDA UDI
K122047 FDA UDI
K140303 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Orthopaedic surgical distractor, internal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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: Orthopaedic surgical distractor, internal

Alamo P, Alamo T by Alliance Partners Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical distractor, internal.

Cleared under the same submission

K120401 also covers:

K122047 also covers:

K140303 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alliance Partners Llc

Sources (1)

  • FDA UDI e2ea6b77-ca3e-4aff-b50c-c2b98d21a9f7 36 fields · synced May 30, 2026