Universal Instrumentation(Cd) for Spinal Surgery

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

510(k) Number

K872715 ↗

FDA Product Code

JDN

Device Class

Class II

Regulation

21 CFR Part 888.3060

Advisory Committee

Orthopedic

FDA Decision

SN

• Spectacle Frame - Danielle

  Class I

  FDA 510(k) K871688 Active Cleared 29 May 1987

• Overshoes (Surchaussures

  Class I

  FDA 510(k) K851554 Active Cleared 30 Apr 1985

• Canal Finder

  Class I

  FDA 510(k) K850294 Active Cleared 4 Jun 1985

• Burnet Laboratoire Pharmaceutique Surgical Gloves

  Class I

  FDA 510(k) K882392 Active Cleared 26 Aug 1988

• Staple, Fixation Bone; Screw Fixation Bone

  Class II

  FDA 510(k) K931155 Active Cleared 1 Sep 1994

• Poirier Kid-Roller Manual Wheelchair

  Class I

  FDA 510(k) K874317 Active Cleared 17 Nov 1987

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