Spine CAMP (1.1)
K-Number: K231668 · 2023-07-07
ApplicantMedical Metrics, Inc.
Decision Date2023-07-07
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Spine CAMP (1.1) is a medical device manufactured by Medical Metrics, Inc.. It received FDA 510(k) clearance on 2023-07-07 under approval number K231668. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Spine CAMP (1.1)?
Spine CAMP (1.1) is a medical device that received FDA 510(k) clearance on 2023-07-07. It is manufactured by Medical Metrics, Inc.. The 510(k) number is K231668.
When was Spine CAMP (1.1) approved by the FDA?
Spine CAMP (1.1) received FDA 510(k) clearance on 2023-07-07, under approval number K231668.
What company makes Spine CAMP (1.1)?
Spine CAMP (1.1) is manufactured by Medical Metrics, Inc..
What is the FDA product code for Spine CAMP (1.1)?
The FDA product code for Spine CAMP (1.1) is QIH.
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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.