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FDA 510(k), K920640, FULL HEMISPHERE RING-LOC LINER
FDA 510(k), K920640, FULL HEMISPHERE RING-LOC LINER
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510(K) Number: K920640
Device Name: FULL HEMISPHERE RING-LOC LINER
Manufacturer: DUTCH HARRISON
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Regulation Number: JDI
Classification Product Code: 02/12/1992
Date Received: 06/30/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: FULL HEMISPHERE RING-LOC LINER
Manufacturer: DUTCH HARRISON
Device Classification Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Regulation Number: JDI
Classification Product Code: 02/12/1992
Date Received: 06/30/1992
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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