GaiaBone Bioabsorbable Bone Graft
K-Number: K220337 · 2023-02-03
Decision Date2023-02-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
GaiaBone Bioabsorbable Bone Graft is a medical device manufactured by Corliber (Shenzhen) Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2023-02-03 under approval number K220337. 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 GaiaBone Bioabsorbable Bone Graft?
GaiaBone Bioabsorbable Bone Graft is a medical device that received FDA 510(k) clearance on 2023-02-03. It is manufactured by Corliber (Shenzhen) Medical Device Co., Ltd.. The 510(k) number is K220337.
When was GaiaBone Bioabsorbable Bone Graft approved by the FDA?
GaiaBone Bioabsorbable Bone Graft received FDA 510(k) clearance on 2023-02-03, under approval number K220337.
What company makes GaiaBone Bioabsorbable Bone Graft?
GaiaBone Bioabsorbable Bone Graft is manufactured by Corliber (Shenzhen) Medical Device Co., Ltd..
What is the FDA product code for GaiaBone Bioabsorbable Bone Graft?
The FDA product code for GaiaBone Bioabsorbable Bone Graft is MQV.
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.