510(k) Submission – NuVasive Precice Intramedullary Limb Lengthening System (K220234)

510(k) Submission – NuVasive Precice Intramedullary Limb Lengthening System (K220234)

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510(K) Number: K220234
Device Name: Precice Intramedullary Limb Lengthening System
Manufacturer: NuVasive Specialized Orthopedics, Inc.
Device Classification Name: Rod, Fixation, Intramedullary And Accessories
Regulation Number: 888.3020
Classification Product Code: HSB
Date Received: 01/27/2022
Decision Date: 03/15/2023
Regulation Medical Specialty: Orthopedic
Request Contents: 510(k) submission of NuVasive for Precice Intramedullary Limb Lengthening System (K220234).
  • 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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