PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G
K-Number: K202475 · 2020-11-23
ApplicantHeraeus Medical GmbH
Decision Date2020-11-23
Product CodeLOD
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G is a medical device manufactured by Heraeus Medical GmbH. It received FDA 510(k) clearance on 2020-11-23 under approval number K202475. 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 PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G?
PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G is a medical device that received FDA 510(k) clearance on 2020-11-23. It is manufactured by Heraeus Medical GmbH. The 510(k) number is K202475.
When was PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G approved by the FDA?
PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G received FDA 510(k) clearance on 2020-11-23, under approval number K202475.
What company makes PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G?
PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G is manufactured by Heraeus Medical GmbH.
What is the FDA product code for PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G?
The FDA product code for PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G is LOD.
Other Devices by Heraeus Medical GmbH
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.