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Minuteman

FDA UDI

Class I (US FDA UDI)

by Spinal Simplicity, LLC

Identity

Trade Name
Minuteman FDA UDI
Generic Name
Orthopaedic implant-instrument extension adaptor, reusable FDA UDI
Device Name
Speed Adapter Hex, Open Sz. 8mm FDA UDI
Model / Reference
20-0094-008 FDA UDI
Description
Speed Adapter Hex, Open Sz. 8mm FDA UDI

Identifiers

Primary DI / UDI-DI
M9432000940080 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant-instrument extension adaptor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant-instrument extension adaptor, reusable

Minuteman by Spinal Simplicity, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant-instrument extension adaptor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spinal Simplicity, LLC

Sources (1)

  • FDA UDI 4c4afb5e-8f40-4a5f-b990-901b114c830c 33 fields · synced Jun 9, 2026