Home / 510(k) Clearances / K972403

510(k) K972403

BTI CORTICAL BONE SCREWS by Biodynamic Technologies, Inc. — Product Code HWC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 29, 1997
Date Received
June 26, 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)
  • K990481 — ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEM (March 17, 1999)
  • K990513 — ULTIMAX CORTICAL BONE SCREWS (March 17, 1999)
  • K981230 — ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEM (June 1, 1998)
  • K980102 — BTI HUMERAL INTRAMEDULLARY ROD SYSTEM (April 3, 1998)
  • K974756 — BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS (March 12, 1998)
  • 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)

Other clearances for product code HWC

  • K260361 — Treace Medical Concepts (TMC) Screw Fixation System (March 6, 2026)
  • K252901 — Tyber Medical Trauma Screw (December 31, 2025)
  • K251555 — Ultra™ Compression Screw System (November 6, 2025)
  • K252312 — Eleganz IM Threaded Nail System (IM Threaded Nail System) (October 10, 2025)
  • K250536 — MetaFore Small Screw System (October 8, 2025)
  • K252758 — Cannulated Screw and Kirschner (K wire) System (October 2, 2025)
  • K252019 — CurvaFix Low Profile System (August 29, 2025)
  • K251382 — Phoenix Sinus Tarsi Stent System (August 27, 2025)
  • K250867 — Dunamis Screw and Suture Locking System (August 15, 2025)
  • K250251 — Eleganz Fusion Screw System (Fusion Screw System) (June 13, 2025)