Bodycad Unicompartmental Knee System
K-Number: K163700 · 2017-03-29
ApplicantBodycad Laboratories, Inc.
Decision Date2017-03-29
Product CodeHSX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Bodycad Unicompartmental Knee System is a medical device manufactured by Bodycad Laboratories, Inc.. It received FDA 510(k) clearance on 2017-03-29 under approval number K163700. The device is classified under product code HSX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bodycad Unicompartmental Knee System?
Bodycad Unicompartmental Knee System is a medical device that received FDA 510(k) clearance on 2017-03-29. It is manufactured by Bodycad Laboratories, Inc.. The 510(k) number is K163700.
When was Bodycad Unicompartmental Knee System approved by the FDA?
Bodycad Unicompartmental Knee System received FDA 510(k) clearance on 2017-03-29, under approval number K163700.
What company makes Bodycad Unicompartmental Knee System?
Bodycad Unicompartmental Knee System is manufactured by Bodycad Laboratories, Inc..
What is the FDA product code for Bodycad Unicompartmental Knee System?
The FDA product code for Bodycad Unicompartmental Knee System is HSX.
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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.