ThoraTrak™

FDA UDI

Class I (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: ThoraTrak™ FDA UDI
Generic Name: Rib spreader, reusable FDA UDI
Device Name: BLADE 28602 THORATRAK LIMA DP FDA UDI
Model / Reference: 28602 FDA UDI
Description: BLADE 28602 THORATRAK LIMA DP FDA UDI

Identifiers

Primary DI / UDI-DI: 00763000058296 FDA UDI
510(k) Number: K132645 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Rib spreader, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Rib spreader, reusable

ThoraTrak™ by Medtronic, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Rib spreader, reusable.

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Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
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Cleared under the same submission

K132645 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 976dd41c-4ae9-4aa3-86a1-c77ab0eb1105 35 fields · synced May 30, 2026