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510(k) K943804

BONE SCREW by Cohort Medical Products Group, Inc. — Product Code HWC

Clearance Details

Decision
SN ()
Decision Date
December 8, 1994
Date Received
August 4, 1994
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 Cohort Medical Products Group, Inc.

  • K964975 — COHORT DISCECTOMY SYSTEMS (CDS) (February 24, 1997)
  • K950011 — COHORT(TM) ANTERIOR PLATE SYSTEM (APS) (November 6, 1995)
  • K943472 — COHORT AVB RETRACTOR SYSTEM (October 20, 1994)
  • K943474 — CANNULATED BONE SCREW (October 14, 1994)

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