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FDA 510(k), K042032, MAESTRO TOTAL WRIST
FDA 510(k), K042032, MAESTRO TOTAL WRIST
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510(K) Number: K042032
Device Name: MAESTRO TOTAL WRIST
Manufacturer: BIOMET, INC.
Device Classification Name: prosthesis, wrist, 3 part metal-plastic-metal articulation, semi-constrained
Regulation Number: 888.3800
Classification Product Code: JWJ
Date Received: 07/28/2004
Decision Date: 10/07/2004
Regulation Medical Specialty: Orthopedic
Device Name: MAESTRO TOTAL WRIST
Manufacturer: BIOMET, INC.
Device Classification Name: prosthesis, wrist, 3 part metal-plastic-metal articulation, semi-constrained
Regulation Number: 888.3800
Classification Product Code: JWJ
Date Received: 07/28/2004
Decision Date: 10/07/2004
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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