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Alamo C

FDA UDI

Class I (US FDA UDI)

by Alliance Partners Llc

Identity

Trade Name
Alamo C FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
Double Ended Trial/Rasp Instrument FDA UDI
Model / Reference
1412T-207 FDA UDI
Description
Double Ended Trial/Rasp Instrument FDA UDI

Identifiers

Catalog Number
1412T-207 FDA UDI
Primary DI / UDI-DI
M6861412T2070 FDA UDI
510(k) Number
K112361 FDA UDI
K173128 FDA UDI
FDA Product Code
HWT FDA UDI
HTR FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
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: Spinal implant trialBone file/rasp, manual, reusable

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

Similar devices

Also classified as Bone file/rasp, manual, reusable.

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 2945b22b-b19d-4323-a151-bb1c48321e4f 37 fields · synced May 30, 2026