Bone Cement-Normal Viscosity
K-Number: K212729 · 2022-05-31
Decision Date2022-05-31
Product CodeLOD
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Bone Cement-Normal Viscosity is a medical device manufactured by Biomecanica Industria E Comerciode Produtos Ortopedicos Ltda. It received FDA 510(k) clearance on 2022-05-31 under approval number K212729. The device is classified under product code LOD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Bone Cement-Normal Viscosity?
Bone Cement-Normal Viscosity is a medical device that received FDA 510(k) clearance on 2022-05-31. It is manufactured by Biomecanica Industria E Comerciode Produtos Ortopedicos Ltda. The 510(k) number is K212729.
When was Bone Cement-Normal Viscosity approved by the FDA?
Bone Cement-Normal Viscosity received FDA 510(k) clearance on 2022-05-31, under approval number K212729.
What company makes Bone Cement-Normal Viscosity?
Bone Cement-Normal Viscosity is manufactured by Biomecanica Industria E Comerciode Produtos Ortopedicos Ltda.
What is the FDA product code for Bone Cement-Normal Viscosity?
The FDA product code for Bone Cement-Normal Viscosity is LOD.
Related Clinical Trials
Related PubMed Literature
Related Devices (Code: LOD)
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.