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Triton®

FDA UDI

Class I (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
Triton® FDA UDI
Generic Name
Surgical power tool system control unit, pneumatic FDA UDI
Device Name
ATT 720106 WIRE COLLET FDA UDI
Model / Reference
720106 FDA UDI
Description
ATT 720106 WIRE COLLET FDA UDI

Identifiers

Primary DI / UDI-DI
00673978033877 FDA UDI
510(k) Number
K870157 FDA UDI
FDA Product Code
KFK FDA UDI
GMDN Term
Surgical power tool system control unit, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical power tool system control unit, pneumatic

Triton® by Medtronic Powered Surgical Solutions — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, pneumatic.

Cleared under the same submission

K870157 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic Powered Surgical Solutions

Sources (1)

  • FDA UDI e726a8f2-14b1-4281-8ae3-8144ca020e9b 35 fields · synced Jun 9, 2026