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510(k) K092017

PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD) by Captiva Spine, Inc. — Product Code MAX

K092017 is an FDA 510(k) premarket notification submitted by Captiva Spine, Inc. for the device "PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)". The FDA issued a decision of Substantially Equivalent on December 1, 2009. The device falls under product code MAX (Intervertebral Fusion Device With Bone Graft, Lumbar), a Class II device regulated under 21 CFR 888.3080. Captiva Spine, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 1, 2009
Date Received
July 6, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class
Class II
Regulation Number
888.3080
Review Panel
OR
Submission Type

Intended to stabilize spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.

Other clearances by Captiva Spine, Inc.

  • K193270 — CapLOX II®/TowerLOX® MIS Pedicle Screw System (January 31, 2020)
  • K181229 — TirboLOX-C Cervical IBFD (September 19, 2018)
  • K180990 — TirboLOX-L Lumbar IBFD (August 13, 2018)
  • K180475 — CapLOX II® / TowerLOX® MIS Pedicle Screw System (March 19, 2018)
  • K160020 — Captiva Spine and CapLOX II/TowerLOX Pedicle Screw System (March 2, 2016)
  • K151116 — CapLOX II/TowerLOX Pedicle Screw System (June 26, 2015)
  • K141332 — Captiva Spine SmartLOX Cervical Plate System (June 11, 2015)
  • K142586 — Captiva Spine FuselOX Cervical IBF System (May 28, 2015)
  • K131538 — CAPLOX II PEDICLE SCREW SYSTEM/TOWERLOX PEDICLE SCREW SYSTEM (August 8, 2013)
  • K122956 — FUSELOX LUMBAR INTERBODY FUSION DEVICE (October 25, 2012)

Other clearances for product code MAX

  • K253011 — Catalyft PL Expandable Interbody System (July 17, 2026)
  • K261020 — Symmetrix™ L Spinal System (July 14, 2026)
  • K253420 — Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Space (July 1, 2026)
  • K253151 — Fule Interbody Fusion Cage System (June 15, 2026)
  • K261159 — Exceed® Biplanar Expandable Interbody System (May 29, 2026)
  • K253894 — BMD Titanium Spinal Fusion System (May 28, 2026)
  • K260506 — Ventana® P/T Lumbar Interbody System (May 15, 2026)
  • K260837 — VersaLift Expandable System (May 12, 2026)
  • K260385 — aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and tran (May 9, 2026)
  • K261067 — BEE PLIF Cage (April 30, 2026)

FDA data resources