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510(k) K040096

SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM by Spinal Concepts, Inc. — Product Code KWP

K040096 is an FDA 510(k) premarket notification submitted by Spinal Concepts, Inc. for the device "SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM". The FDA issued a decision of Substantially Equivalent on July 1, 2004. The device falls under product code KWP (Appliance, Fixation, Spinal Interlaminal), a Class II device regulated under 21 CFR 888.3050. Spinal Concepts, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 1, 2004
Date Received
January 20, 2004
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 Spinal Concepts, Inc.

  • K051000 — FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE (May 19, 2005)
  • K050706 — HARMONY PORT SYSTEM, MODEL 1907 SERIES (April 15, 2005)
  • K033663 — SPINAL CONCEPTS INC. CODA (May 27, 2004)
  • K033517 — SPINAL CONCEPTS INC. CADENCE AND TRAXIS (February 18, 2004)
  • K031855 — SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM (September 17, 2003)
  • K031985 — SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM (September 11, 2003)
  • K031318 — TRAXIS CEMENT RESTRICTOR (August 22, 2003)
  • K031672 — SPINAL CONCEPTS, INC. INFIX SYSTEM (August 7, 2003)
  • K031837 — MODIFICATION TO FORTITUDE CEMENT RESTRICTOR (July 24, 2003)
  • K030087 — SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM (July 17, 2003)

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