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Spider Single Port Surgical Device, Support Arm Accessory, Model 90001, 90002, 90003

by Transenterix, Inc.

510(k) K090902

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 · Traditional NumberK090902 Date22 Jul 2009ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-1909-2011 FDA Unclassified (pre-2012) initiated 25 Feb 2011

    Plastic shards may break off and fall into the abdominal space which may require retrieval during surgery.

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  • Withdrawn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
GCJ
Models / Variants
Device Class
Class II
Regulation
21 CFR Part 876.1500
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

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