Bicera Resorbable Bone Substitute
K-Number: K172237 · 2018-02-02
ApplicantWiltrom Corporation Limited
Decision Date2018-02-02
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Bicera Resorbable Bone Substitute is a medical device manufactured by Wiltrom Corporation Limited. It received FDA 510(k) clearance on 2018-02-02 under approval number K172237. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bicera Resorbable Bone Substitute?
Bicera Resorbable Bone Substitute is a medical device that received FDA 510(k) clearance on 2018-02-02. It is manufactured by Wiltrom Corporation Limited. The 510(k) number is K172237.
When was Bicera Resorbable Bone Substitute approved by the FDA?
Bicera Resorbable Bone Substitute received FDA 510(k) clearance on 2018-02-02, under approval number K172237.
What company makes Bicera Resorbable Bone Substitute?
Bicera Resorbable Bone Substitute is manufactured by Wiltrom Corporation Limited.
What is the FDA product code for Bicera Resorbable Bone Substitute?
The FDA product code for Bicera Resorbable Bone Substitute is MQV.
Other Devices by Wiltrom Corporation Limited
Related Devices (Code: MQV)
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.