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510(k) K951702

FMS HIGH FLOW ARTHRO-SHEATH by Future Medical Systems, Inc. — Product Code HNX

Clearance Details

Decision
SN ()
Decision Date
May 12, 1995
Date Received
April 12, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Depressor, Orbital
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type

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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)

Other clearances for product code HNX

  • K951701 — FMS ARTHRO-CUTTER (May 9, 1995)