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FDA 510(k), K030861, HA PMI FLANGED ACETABULAR COMPONENT
FDA 510(k), K030861, HA PMI FLANGED ACETABULAR COMPONENT
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510(K) Number: K030861
Device Name: HA PMI FLANGED ACETABULAR COMPONENT
Manufacturer: BIOMET, INC.
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 03/18/2003
Decision Date: 06/12/2003
Regulation Medical Specialty: Orthopedic
Device Name: HA PMI FLANGED ACETABULAR COMPONENT
Manufacturer: BIOMET, INC.
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 03/18/2003
Decision Date: 06/12/2003
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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