Identity
- Trade Name
- TurboHawk FDA UDI
- Generic Name
- Mechanical atherectomy system catheter, peripheral FDA UDI
- Device Name
- Peripheral Plaque Excision System;Large Vessel Xtended Tip with MEC TechNlogy FDA UDI
- Model / Reference
- TH-LX-M FDA UDI
- Description
- Peripheral Plaque Excision System;Large Vessel Xtended Tip with MEC TechNlogy FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00821684047149 FDA UDI
- 510(k) Number
- K111723 FDA UDI
- FDA Product Code
- MCW FDA UDI
- GMDN Term
- Mechanical atherectomy system catheter, peripheral FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4875 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 2.7 Millimeter FDA UDILength — 9.0 Centimeter FDA UDICatheter Gauge — 8 French FDA UDI
Category: Mechanical atherectomy system catheter, peripheral
TurboHawk by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Mechanical atherectomy system catheter, peripheral.
- Stealth — Cardiovascular Systems, Inc. · Class II
- Kittykat II — AVINGER, INC. · Class II
- DIAMONDBACK — Cardiovascular Systems, Inc. · Class II
- Stealth — Cardiovascular Systems, Inc. · Class II
- Diamondback Peripheral — Cardiovascular Systems, Inc. · Class II
- Stealth — Cardiovascular Systems, Inc. · Class II
- Diamondback Peripheral — Cardiovascular Systems, Inc. · Class II
- Lightbox L3 — AVINGER, INC. · Class II
Cleared under the same submission
K111723 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Covidien LP
Sources (1)
- FDA UDI 9e71ca8a-1019-436b-aa70-98ee2cfa4ba6 37 fields · synced Jun 8, 2026