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Everest 20 Inflation Device and 3-way Stopcock (AC2200) +3 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K220773

by Medtronic Vascular

Identifiers

510(k) Number
K220773 FDA 510(k)
FDA Product Code
MAV FDA 510(k)
Models / Variants
Everest 20 Inflation Device and 3-way Stopcock (AC2200) FDA 510(k)
Everest 30 Inflation Device and 3-way Stopcock (AC3200) FDA 510(k)
Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor , 3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P) FDA 510(k)
Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor, 3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 870.1650 FDA 510(k)
Regulation Number
870.1650 FDA 510(k)
Advisory Committee
Cardiovascular FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Everest 20 Inflation Device and 3-way Stopcock (AC2200) +3 more models by Medtronic Vascular — Class II — FDA_510K — listed in FDA 510(k) — 4 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Medtronic Vascular

Sources (1)

  • FDA 510(k) K220773 24 fields · synced Oct 9, 2026