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FDA 510(k)

DISCOVERY

K-Number: K111484 · 2011-09-12

ApplicantIntuitive Spine, LLC
Decision Date2011-09-12
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DISCOVERY is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Spine, LLC. It received FDA 510(k) clearance on 2011-09-12 under 510(k) number K111484. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCOVERY?

DISCOVERY is a medical device that received FDA 510(k) clearance on 2011-09-12. The listed applicant is Intuitive Spine, LLC. The 510(k) number is K111484.

When did DISCOVERY receive FDA 510(k) clearance?

DISCOVERY received FDA 510(k) clearance on 2011-09-12, under 510(k) number K111484.

Who is the listed applicant for DISCOVERY?

The FDA 510(k) record lists Intuitive Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISCOVERY?

The FDA product code for DISCOVERY is ODP.

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Related Devices (Code: ODP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262595VariLift-C Cervical Interbody Fusion SystemWenzel Spine, Inc.K262489BluEX Cervical Expandable Cage SystemL&K BIOMED Co., Ltd.K2530413d Cage CervicalFims Co., Ltd.K262061Tritanium® C Anterior Cervical Cage; Tritanium® PL Cage; Tritanium® TL Curved Posterior Lumbar Cage; Aero® -C Cervical Cage System; AVS® Anchor-C Cervical Cage System; AVS® TL PEEK Spacer; AVS® PL PEEK Spacers; AVS® Navigator PEEK Spacer; AVS® AS PEEK Spacer; Monterey™ AL Interbody System; Aleutian IBF System; Cascadia Interbody System; Chesapeake Stabilization System; Sahara Stabilization System; SANTORINI™ Corpectomy Cage System; MOJAVE Interbody System; VLIFT VERTEBRAL BODY REPLACEMStryker SpineK254130C.A. Medical Interbody Fusion SystemC.A. Medical, LLCK260840BluEX Cervical Expandable Cage SystemL&K BIOMED Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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