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FDA 510(k), K042037, M2A MAGNUM SYSTEM
FDA 510(k), K042037, M2A MAGNUM SYSTEM
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510(K) Number: K042037
Device Name: M2A MAGNUM SYSTEM
Manufacturer: BIOMET, INC.
Device Classification Name: prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Regulation Number: 888.3330
Classification Product Code: KWA
Date Received: 07/29/2004
Decision Date: 10/01/2004
Regulation Medical Specialty: Orthopedic
Device Name: M2A MAGNUM SYSTEM
Manufacturer: BIOMET, INC.
Device Classification Name: prosthesis, hip, semi-constrained (metal uncemented acetabular component)
Regulation Number: 888.3330
Classification Product Code: KWA
Date Received: 07/29/2004
Decision Date: 10/01/2004
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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