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FDA 510(k), K071160, REFLECTION, TANDEM UNIPOLAR
FDA 510(k), K071160, REFLECTION, TANDEM UNIPOLAR
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510(K) Number: K071160
Device Name: REFLECTION, TANDEM UNIPOLAR
Manufacturer: SMITH & NEPHEW, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 04/26/2007
Decision Date: 10/05/2007
Regulation Medical Specialty: Orthopedic
Device Name: REFLECTION, TANDEM UNIPOLAR
Manufacturer: SMITH & NEPHEW, INC.
Device Classification Name: prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Regulation Number: 888.3358
Classification Product Code: LPH
Date Received: 04/26/2007
Decision Date: 10/05/2007
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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