SALVATION Midfoot Nail
K-Number: K180024 · 2018-07-11
ApplicantWrightmedicaltechnologyinc
Decision Date2018-07-11
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
SALVATION Midfoot Nail is a medical device manufactured by Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2018-07-11 under approval number K180024. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the SALVATION Midfoot Nail?
SALVATION Midfoot Nail is a medical device that received FDA 510(k) clearance on 2018-07-11. It is manufactured by Wrightmedicaltechnologyinc. The 510(k) number is K180024.
When was SALVATION Midfoot Nail approved by the FDA?
SALVATION Midfoot Nail received FDA 510(k) clearance on 2018-07-11, under approval number K180024.
What company makes SALVATION Midfoot Nail?
SALVATION Midfoot Nail is manufactured by Wrightmedicaltechnologyinc.
What is the FDA product code for SALVATION Midfoot Nail?
The FDA product code for SALVATION Midfoot Nail is HWC. This falls under the Cardiovascular category.
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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.