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FDA 510(k), K143314, Progressive Orthopaedic Total Hip System
FDA 510(k), K143314, Progressive Orthopaedic Total Hip System
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510(K) Number: K143314
Device Name: Progressive Orthopaedic Total Hip System
Manufacturer: The Progressive Orthopaedic Company, LLC
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 11/19/2014
Decision Date: 02/27/2015
Regulation Medical Specialty: Orthopedic
Device Name: Progressive Orthopaedic Total Hip System
Manufacturer: The Progressive Orthopaedic Company, LLC
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 11/19/2014
Decision Date: 02/27/2015
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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