FDA 510(k), K894184, BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM

FDA 510(k), K894184, BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM

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510(K) Number: K894184
Device Name: BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM
Manufacturer: BIEDERMANN MOTECH GMBH
Device Classification Name: implant, fixation device, spinal
Regulation Number: 888.3060
Classification Product Code: JDN
Date Received: 06/16/1989
Decision Date: 04/25/1990
Regulation Medical Specialty: Orthopedic
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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