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FDA 510(k), K073570, DEPUY TRI-LOCK BONE PRESERVATION STEM
FDA 510(k), K073570, DEPUY TRI-LOCK BONE PRESERVATION STEM
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510(K) Number: K073570
Device Name: DEPUY TRI-LOCK BONE PRESERVATION STEM
Manufacturer: RHONDA MYER
Device Classification Name: Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Regulation Number: KWA
Classification Product Code: 12/20/2007
Date Received: 02/21/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: DEPUY TRI-LOCK BONE PRESERVATION STEM
Manufacturer: RHONDA MYER
Device Classification Name: Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
Regulation Number: KWA
Classification Product Code: 12/20/2007
Date Received: 02/21/2008
Decision Date: Substantially Equivalent (SESE)
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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