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510(k) K013685

PLLA CANNULATED INTERFERENCE SCREW by Future Medical Systems, Inc. — Product Code HWC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 18, 2002
Date Received
November 7, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Screw, Fixation, Bone
Device Class
Class II
Regulation Number
888.3040
Review Panel
OR
Submission Type

Other clearances by Future Medical Systems, Inc.

  • K041824 — X-TREME ARTHROSCOPIC PUMP AND SHAVER SYSTEM (January 7, 2005)
  • K024185 — BIODHOC (January 15, 2004)
  • K023963 — ADHOC CLAW (May 5, 2003)
  • K021030 — TITANIUM CANNULATED INTERFERENCE SCREW (June 25, 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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