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510(k) K850039

HALIFAX SPINAL CLAMP by Levtech, Inc. — Product Code KWP

K850039 is an FDA 510(k) premarket notification submitted by Levtech, Inc. for the device "HALIFAX SPINAL CLAMP". The FDA issued a decision of Substantially Equivalent on May 29, 1985. The device falls under product code KWP (Appliance, Fixation, Spinal Interlaminal), a Class II device regulated under 21 CFR 888.3050. Levtech, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 29, 1985
Date Received
January 7, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Appliance, Fixation, Spinal Interlaminal
Device Class
Class II
Regulation Number
888.3050
Review Panel
OR
Submission Type

Other clearances by Levtech, Inc.

  • K910128 — LEVTECH TITANIUM BONE WIRE (June 18, 1991)
  • K901144 — LEVTECH BONE SCREW (October 10, 1990)
  • K873693 — LEVTECH COMPOSITE TRACTION TONGS (February 5, 1988)
  • K874023 — LEVTECH CLAMP APPLIER (November 6, 1987)

Other clearances for product code KWP

  • K143278 — LnK Posterior Cervical Fixation System (July 29, 2015)
  • K150753 — OASYS System (June 9, 2015)
  • K150851 — Sure Lok Mini Posterior Cervical/Upper Thoracic System (June 4, 2015)
  • K142867 — Reliance Posterior Cervical-Thoracic System (April 29, 2015)
  • K150254 — Streamline OCT Occipito-Cervico-Thoracic System (April 28, 2015)
  • K142253 — SOLSTICE OCT System (April 23, 2015)
  • K143249 — SOLSTICE OCT System (April 7, 2015)
  • K150229 — SOLSTICE OCT System (April 7, 2015)
  • K142741 — OASYS System (January 15, 2015)
  • K142558 — Caspian OCT/MESA Mini/DENALI Mini Spinal System (December 22, 2014)

FDA data resources