Alliance Glenoid
K-Number: K191814 · 2019-10-23
ApplicantZimmer, Inc.
Decision Date2019-10-23
Product CodeKWS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Alliance Glenoid is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2019-10-23 under approval number K191814. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Alliance Glenoid?
Alliance Glenoid is a medical device that received FDA 510(k) clearance on 2019-10-23. It is manufactured by Zimmer, Inc.. The 510(k) number is K191814.
When was Alliance Glenoid approved by the FDA?
Alliance Glenoid received FDA 510(k) clearance on 2019-10-23, under approval number K191814.
What company makes Alliance Glenoid?
Alliance Glenoid is manufactured by Zimmer, Inc..
What is the FDA product code for Alliance Glenoid?
The FDA product code for Alliance Glenoid is KWS.
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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.