NGM WAVE PLIF Cage
K-Number: K212050 · 2021-12-01
ApplicantNGMedical GmbH
Decision Date2021-12-01
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
NGM WAVE PLIF Cage is a medical device manufactured by NGMedical GmbH. It received FDA 510(k) clearance on 2021-12-01 under approval number K212050. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NGM WAVE PLIF Cage?
NGM WAVE PLIF Cage is a medical device that received FDA 510(k) clearance on 2021-12-01. It is manufactured by NGMedical GmbH. The 510(k) number is K212050.
When was NGM WAVE PLIF Cage approved by the FDA?
NGM WAVE PLIF Cage received FDA 510(k) clearance on 2021-12-01, under approval number K212050.
What company makes NGM WAVE PLIF Cage?
NGM WAVE PLIF Cage is manufactured by NGMedical GmbH.
What is the FDA product code for NGM WAVE PLIF Cage?
The FDA product code for NGM WAVE PLIF Cage is MAX.
Other Devices by NGMedical GmbH
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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.