StageOne Knee Cement Spacer Molds
K-Number: K213287 · 2022-09-02
Device Summary
Frequently Asked Questions
What is the StageOne Knee Cement Spacer Molds?
StageOne Knee Cement Spacer Molds is a medical device that received FDA 510(k) clearance on 2022-09-02. It is manufactured by Biomet, Inc.. The 510(k) number is K213287.
When was StageOne Knee Cement Spacer Molds approved by the FDA?
StageOne Knee Cement Spacer Molds received FDA 510(k) clearance on 2022-09-02, under approval number K213287.
What company makes StageOne Knee Cement Spacer Molds?
StageOne Knee Cement Spacer Molds is manufactured by Biomet, Inc..
What is the FDA product code for StageOne Knee Cement Spacer Molds?
The FDA product code for StageOne Knee Cement Spacer Molds is MBB.
Other Devices by Biomet, Inc.
Related Devices (Code: MBB)
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.