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Midas Rex Legend

FDA UDI

Class II (US FDA UDI)

by Medtronic Powered Surgical Solutions

Identity

Trade Name
MIDAS REX LEGEND FDA UDI
Generic Name
Orthopaedic bur, single-use FDA UDI
Device Name
TOOL 7BA50F-MN LEGEND 7CM 5MM BA FI MN FDA UDI
Model / Reference
7BA50F-MN FDA UDI
Description
TOOL 7BA50F-MN LEGEND 7CM 5MM BA FI MN FDA UDI

Identifiers

Primary DI / UDI-DI
00763000061678 FDA UDI
510(k) Number
K020069 FDA UDI
K170312 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Orthopaedic bur, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4370 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

Midas Rex Legend by Medtronic Powered Surgical Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bur, single-use.

Cleared under the same submission

K020069 also covers:

K170312 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 76290086-44d2-4edd-9b29-0d655e1a77d2 35 fields · synced Jun 9, 2026