WaveForm A Interbody System
K-Number: K222732 · 2022-11-07
ApplicantSeaSpine Orthopedics Corporation
Decision Date2022-11-07
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
WaveForm A Interbody System is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2022-11-07 under approval number K222732. 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 WaveForm A Interbody System?
WaveForm A Interbody System is a medical device that received FDA 510(k) clearance on 2022-11-07. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K222732.
When was WaveForm A Interbody System approved by the FDA?
WaveForm A Interbody System received FDA 510(k) clearance on 2022-11-07, under approval number K222732.
What company makes WaveForm A Interbody System?
WaveForm A Interbody System is manufactured by SeaSpine Orthopedics Corporation.
What is the FDA product code for WaveForm A Interbody System?
The FDA product code for WaveForm A Interbody System is MAX.
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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.