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510(k) K102020

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM by Spinefrontier, Inc. — Product Code KWP

K102020 is an FDA 510(k) premarket notification submitted by Spinefrontier, Inc. for the device "VEGA SPAN SPINOUS PROCESS PLATE SYSTEM". The FDA issued a decision of Substantially Equivalent on September 1, 2010. The device falls under product code KWP (Appliance, Fixation, Spinal Interlaminal), a Class II device regulated under 21 CFR 888.3050. Spinefrontier, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 1, 2010
Date Received
July 19, 2010
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 Spinefrontier, Inc.

  • K193106 — SpineFrontier Lumbar Interbody Fusion Device System (June 19, 2020)
  • K172484 — A-CIFT SoloFuse (May 8, 2018)
  • K151198 — A-CIFT SoloFuse (July 17, 2015)
  • K142504 — SpineFrontier Lumbar Interbody Fusion Device System (May 13, 2015)
  • K150017 — SpineFrontier SIJFuse Sacroiliac Joint Fusion Device System (April 24, 2015)
  • K143377 — PedFuse Pedicle Screw System (February 12, 2015)
  • K141333 — ARENA-C TIFUSE CERVICAL INTERVERTEBRAL BODY FUSION DEVICE (November 25, 2014)
  • K142026 — SPINEFRONTIER ARENA-C HA PEEK CERVICAL INTERVERTEBRAL BODY FUSION DEVICE (October 20, 2014)
  • K141337 — ARENA-C (September 8, 2014)
  • K133153 — SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM (May 14, 2014)

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