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510(k) K024185

BIODHOC by Future Medical Systems, SA — Product Code HTY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 15, 2004
Date Received
December 19, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pin, Fixation, Smooth
Device Class
Class II
Regulation Number
888.3040
Review Panel
OR
Submission Type

Other clearances by Future Medical Systems, SA

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  • K021030 — TITANIUM CANNULATED INTERFERENCE SCREW (June 25, 2002)
  • K013685 — PLLA CANNULATED INTERFERENCE SCREW (January 18, 2002)
  • K002040 — FMS SOLO (September 11, 2000)
  • K980808 — ENDO FMS UROLOGY (May 8, 1998)
  • K955500 — FMS ARTHOPROBE (February 5, 1996)
  • K954465 — FMS DUO (November 9, 1995)
  • K954217 — ARTHROPLAST & ARTHRO-CUTTER (October 23, 1995)
  • K951843 — REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT (July 14, 1995)

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