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Surgical Spring Clips

by Applied Vascular Devices, Inc.

510(k) K883909

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

4 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK883909 Date27 Dec 1988ClearedStatusActive

Recalls

4 recalls · FDA

  • 4 recalls, same reason

    • Terminated Z-2035-2020 FDA Class II initiated 31 Jan 2020
    • Terminated Z-2037-2020 FDA Class II initiated 31 Jan 2020
    • Terminated Z-2034-2020 FDA Class II initiated 31 Jan 2020
    • Terminated Z-2036-2020 FDA Class II initiated 31 Jan 2020

    Failure of cardiovascular clips to provide sufficient occlusion of the vessel.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DSS
Device Class
Class II
Regulation
21 CFR Part 870.3250
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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