Disposable Perforator

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K924242 ↗

FDA Product Code

HBF

Device Class

Class II

Regulation

21 CFR Part 882.4305

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K902257 Active Cleared 19 Jul 1990

• Orbit Galaxy G2 Microcoil Delivery System

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• Vanderbilt Pituitary Retractor

  Class I

  FDA 510(k) K761096 Active Cleared 30 Nov 1976

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  Class II

  FDA 510(k) K083895 Active Cleared 23 Jun 2009

See all devices from Codman & Shurtleff, Inc. →