FDA 510(k), K070560, LRTM SURGICAL MESH

FDA 510(k), K070560, LRTM SURGICAL MESH

Regular price $49.00 USD
Regular price Sale price $49.00 USD
Sale Sold out
510(K) Number: K070560
Device Name: LRTM SURGICAL MESH
Manufacturer: LIFECELL CORP.
Device Classification Name: Mesh, Surgical
Regulation Number: 878.3300
Classification Product Code: FTM
Date Received: 02/27/2007
Decision Date: 06/11/2007
Regulation Medical Specialty: General & Plastic Surgery
  • 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.

View full details