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Spinesmith Cynch Spinal System - Visualif Interbody Fusion Implant System

by Spine Smith Partners L.P.

510(k) K102090

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 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 · Special NumberK102090 Date30 Sep 2010ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-2258-2013 FDA Class II initiated 31 Jul 2013 on shared 510(k) K102090

    The product has the potential to be laser marked as a Medium when it actually is a Small.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

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  • Withdrawn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
OVD
Device Class
Class II
Regulation
21 CFR Part 888.3080
Advisory Committee
Orthopedic
FDA Decision
SESE Substantially Equivalent

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