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Distal Cut Adaptor

FDA UDI

Class I (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Distal Cut Adaptor FDA UDI
Generic Name
Orthopaedic implant-instrument extension adaptor, reusable FDA UDI
Model / Reference
122-16-0245 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215031633 FDA UDI
510(k) Number
K181338 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Orthopaedic implant-instrument extension adaptor, reusable 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 implant-instrument extension adaptor, reusable

Distal Cut Adaptor by Signature Orthopaedics Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant-instrument extension adaptor, 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 3a6cb7b6-97e8-4cf4-8d83-2bfae49d85ed 33 fields · synced Jun 1, 2026