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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: KXA
Date Received: 02/12/1992
Decision Date: 06/30/1992
Decision: 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: KXA
Date Received: 02/12/1992
Decision Date: 06/30/1992
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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