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Endoscopic Mortons Neuroma Instruments

by Instratek, Inc.

510(k) K940230

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

13 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 NumberK940230 Date12 Dec 1994ClearedStatusActive

Recalls

13 recalls · FDA

  • 13 recalls, same reason

    • Terminated Z-2414-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2421-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2413-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2420-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2416-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2412-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2418-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2419-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2417-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2423-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2415-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2422-2019 FDA Class II initiated 25 Jul 2019
    • Terminated Z-2424-2019 FDA Class II initiated 25 Jul 2019

    The seal integrity of the sterile bag containing the kits may be compromised.

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  • Withdrawn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
HRX
Device Class
Class II
Regulation
21 CFR Part 888.1100
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

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