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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
Orthopaedic bur, single-use FDA UDI
Device Name
BLADE 252R1RS TRITON RECIP 9.4MMX39.1MM FDA UDI
Model / Reference
252R1RS FDA UDI
Description
BLADE 252R1RS TRITON RECIP 9.4MMX39.1MM FDA UDI

Identifiers

Primary DI / UDI-DI
00673978966205 FDA UDI
510(k) Number
K870157 FDA UDI
FDA Product Code
KFK FDA UDI
GMDN Term
Orthopaedic bur, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Category: Orthopaedic bur, single-use

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

Similar devices

Also classified as Orthopaedic bur, single-use.

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 579747c1-38af-4c9f-866a-e958e9b61dd5 35 fields · synced Jun 9, 2026