Arthrex VaultLock Glenoid

by Arthrex, Inc.

510(k) K161108

Arthrex VaultLock Glenoid is a Class II device made by Arthrex, Inc., cleared under FDA 510(k) K161108 on 29 Aug 2016, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K161108↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK161108	Date29 Aug 2016Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K161108

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K161108
FDA product code: KWS

Device class: Class II
Regulation: 21 CFR Part 888.3660
Advisory committee: Orthopedic
FDA decision: SESE Substantially Equivalent

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