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 a medical device manufactured by Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2017-09-07 under approval 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. It is manufactured by Reliance Medical Systems, LLC. The 510(k) number is K172489.
When was Reliance Cervical IBF System approved by the FDA?
Reliance Cervical IBF System received FDA 510(k) clearance on 2017-09-07, under approval number K172489.
What company makes Reliance Cervical IBF System?
Reliance Cervical IBF System is manufactured by Reliance Medical Systems, LLC.
What is the FDA product code for Reliance Cervical IBF System?
The FDA product code for Reliance Cervical IBF System is ODP.
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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.