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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 knife FDA UDI
Device Name
Paddle Shaver Instrument FDA UDI
Model / Reference
2100T-1613 FDA UDI
Description
Paddle Shaver Instrument FDA UDI

Identifiers

Catalog Number
2100T-1613 FDA UDI
Primary DI / UDI-DI
M6862100T16130 FDA UDI
510(k) Number
K120401 FDA UDI
K122047 FDA UDI
K140303 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Orthopaedic knife 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 knife

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 knife.

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 348c0cc8-bf32-4416-afef-b7bfbef87c7b 37 fields · synced Jun 1, 2026