510(k) K220337
K220337 is an FDA 510(k) premarket notification submitted by Corliber (Shenzhen) Medical Device Co., Ltd. for the device "GaiaBone Bioabsorbable Bone Graft". The FDA issued a decision of Substantially Equivalent on Feb 3, 2023. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 3, 2023
- Date Received
- Feb 7, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Filler, Bone Void, Calcium Compound
- Device Class
- Class II
- Regulation Number
- 888.3045
- Review Panel
- OR
- Submission Type
- 510(k)