KLS Martin Level One Rib Fixation System
K-Number: K222397 · 2023-03-29
ApplicantKLS-Martin L.P.
Decision Date2023-03-29
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
KLS Martin Level One Rib Fixation System is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2023-03-29 under approval number K222397. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the KLS Martin Level One Rib Fixation System?
KLS Martin Level One Rib Fixation System is a medical device that received FDA 510(k) clearance on 2023-03-29. It is manufactured by KLS-Martin L.P.. The 510(k) number is K222397.
When was KLS Martin Level One Rib Fixation System approved by the FDA?
KLS Martin Level One Rib Fixation System received FDA 510(k) clearance on 2023-03-29, under approval number K222397.
What company makes KLS Martin Level One Rib Fixation System?
KLS Martin Level One Rib Fixation System is manufactured by KLS-Martin L.P..
What is the FDA product code for KLS Martin Level One Rib Fixation System?
The FDA product code for KLS Martin Level One Rib Fixation System is HRS.
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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.