MUTARS® femoral stem cemented 160 mm and 200 mm
K-Number: K240391 · 2024-10-24
ApplicantImplantcast GmbH
Decision Date2024-10-24
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MUTARS® femoral stem cemented 160 mm and 200 mm is a medical device manufactured by Implantcast GmbH. It received FDA 510(k) clearance on 2024-10-24 under approval number K240391. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MUTARS® femoral stem cemented 160 mm and 200 mm?
MUTARS® femoral stem cemented 160 mm and 200 mm is a medical device that received FDA 510(k) clearance on 2024-10-24. It is manufactured by Implantcast GmbH. The 510(k) number is K240391.
When was MUTARS® femoral stem cemented 160 mm and 200 mm approved by the FDA?
MUTARS® femoral stem cemented 160 mm and 200 mm received FDA 510(k) clearance on 2024-10-24, under approval number K240391.
What company makes MUTARS® femoral stem cemented 160 mm and 200 mm?
MUTARS® femoral stem cemented 160 mm and 200 mm is manufactured by Implantcast GmbH.
What is the FDA product code for MUTARS® femoral stem cemented 160 mm and 200 mm?
The FDA product code for MUTARS® femoral stem cemented 160 mm and 200 mm is LZO.
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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.