Mayfield Radiolucent Skull Clamp

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K934289 ↗

FDA Product Code

HBL

Device Class

Class II

Regulation

21 CFR Part 882.4460

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Cuddle Up Pillow

  Class I

  FDA 510(k) K882544 Active Cleared 31 Jan 1989

• Mayfield Adult Disposable Skull Pin

  Class II

  FDA 510(k) K932860 Active Cleared 28 Sep 1993

• The Mayfield / Acciss System with Windows Nt for Cranial Surgery, the Mayfield / Optical Acciss System with Windows Nt F

  Class II

  FDA 510(k) K992843 Active Cleared 2 Nov 1999

• Mayfield Acciss Optical System

  Class II

  FDA 510(k) K982244 Active Cleared 23 Sep 1998

• Budde-Halo Retractor

  Class II

  FDA 510(k) K830332 Active Cleared 2 Mar 1983

• Mayfield Table-Electric

  Class I

  FDA 510(k) K851021 Active Cleared 21 May 1985

See all devices from Ohio Medical Instrument Co., Inc. →