FDA 510(k) Application Details - K920739

Device Classification Name Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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510(K) Number K920739
Device Name Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Applicant JOINT MEDICAL PRODUCTS CORP.
860 CANAL ST.
STAMFORD, CT US
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Contact DEBRA L BING
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Regulation Number 888.3350

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Classification Product Code JDI
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Date Received 02/19/1992
Decision Date 11/24/1992
Decision SN - Substantially Equivalent for Some Indications
Classification Advisory Committee OR - Orthopedic
Review Advisory Committee OR - Orthopedic
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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