FDA 510(k), K062181, C-JAWS CERVICAL COMPRESSIVE MINI FRAME

FDA 510(k), K062181, C-JAWS CERVICAL COMPRESSIVE MINI FRAME

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510(K) Number: K062181
Device Name: C-JAWS CERVICAL COMPRESSIVE MINI FRAME
Manufacturer: MEDICREA TECHNOLOGIES
Device Classification Name: appliance, fixation, spinal interlaminal
Regulation Number: 888.3050
Classification Product Code: KWP
Date Received: 07/31/2006
Decision Date: 01/16/2007
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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