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FDA 510(k)

Reliance Cervical IBF System

K-Number: K172489 · 2017-09-07

ApplicantReliance Medical Systems, LLC
Decision Date2017-09-07
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Reliance Cervical IBF System is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2017-09-07 under 510(k) number K172489. 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 Reliance Cervical IBF System?

Reliance Cervical IBF System is a medical device that received FDA 510(k) clearance on 2017-09-07. The listed applicant is Reliance Medical Systems, LLC. The 510(k) number is K172489.

When did Reliance Cervical IBF System receive FDA 510(k) clearance?

Reliance Cervical IBF System received FDA 510(k) clearance on 2017-09-07, under 510(k) number K172489.

Who is the listed applicant for Reliance Cervical IBF System?

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

What is the FDA product code for Reliance Cervical IBF System?

The FDA product code for Reliance Cervical IBF System is ODP.

Other records listing Reliance Medical Systems, LLC as applicant

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.

K202266Reliance Cervical IBF SystemK210874Reliance Spinal Screw SystemK183049Reliance Lumbar IBF SystemK181118Reliance Lumbar IBF SystemK180687Reliance Lumber IBF SystemK173283Reliance Lumbar IBF System

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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.

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.K260850OSTEOMNI SPINAL CAGES SYSTEMOsteomni, Inc.K260549ZSFab Cervical Interbody System and ZSFab Lumbar Interbody SystemZsfab, Inc.

Official Source

View on FDA Database →

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

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