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510(k) K974756

BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS by Biodynamic Technologies, Inc. — Product Code HWC

Clearance Details

Decision
SN ()
Decision Date
March 12, 1998
Date Received
December 19, 1997
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 Biodynamic Technologies, Inc.

  • K990436 — ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM (March 31, 1999)
  • K990513 — ULTIMAX CORTICAL BONE SCREWS (March 17, 1999)
  • K990481 — ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM (March 17, 1999)
  • K981230 — ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM (June 1, 1998)
  • K980102 — BTI HUMERAL INTRAMEDULLARY ROD SYSTEM (April 3, 1998)
  • K972403 — BTI CORTICAL BONE SCREWS (August 29, 1997)
  • K970897 — BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM (April 21, 1997)
  • K962706 — EZ-FIX CANNULATED SCREW SYSTEM (November 13, 1996)
  • K962987 — EZ-FIX SMALL CANNULATED SCREW SYSTEM (November 4, 1996)
  • K962846 — EZ-FIX COMPRESSION HIP/SUPRACONDYLAR SCREW (CHS) SYSTEM (October 23, 1996)

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