SPIRA Open Matrix ALIF
K-Number: K162986 · 2017-06-12
ApplicantCamber Spine Technologies
Decision Date2017-06-12
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
SPIRA Open Matrix ALIF is a medical device manufactured by Camber Spine Technologies. It received FDA 510(k) clearance on 2017-06-12 under approval number K162986. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SPIRA Open Matrix ALIF?
SPIRA Open Matrix ALIF is a medical device that received FDA 510(k) clearance on 2017-06-12. It is manufactured by Camber Spine Technologies. The 510(k) number is K162986.
When was SPIRA Open Matrix ALIF approved by the FDA?
SPIRA Open Matrix ALIF received FDA 510(k) clearance on 2017-06-12, under approval number K162986.
What company makes SPIRA Open Matrix ALIF?
SPIRA Open Matrix ALIF is manufactured by Camber Spine Technologies.
What is the FDA product code for SPIRA Open Matrix ALIF?
The FDA product code for SPIRA Open Matrix ALIF is MAX.
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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.