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FDA 510(k), K812672, SELF-CENTERING HIP
FDA 510(k), K812672, SELF-CENTERING HIP
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510(K) Number: K812672
Device Name: SELF-CENTERING HIP
Manufacturer:
Device Classification Name: Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Regulation Number: KWY
Classification Product Code: 09/22/1981
Date Received: 10/08/1981
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: SELF-CENTERING HIP
Manufacturer:
Device Classification Name: Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Regulation Number: KWY
Classification Product Code: 09/22/1981
Date Received: 10/08/1981
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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