CaP Spheres Pellet Pack
K-Number: K203218 · 2021-05-04
ApplicantZimmer Biomet Spine, Inc.
Decision Date2021-05-04
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CaP Spheres Pellet Pack is a medical device manufactured by Zimmer Biomet Spine, Inc.. It received FDA 510(k) clearance on 2021-05-04 under approval number K203218. 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 CaP Spheres Pellet Pack?
CaP Spheres Pellet Pack is a medical device that received FDA 510(k) clearance on 2021-05-04. It is manufactured by Zimmer Biomet Spine, Inc.. The 510(k) number is K203218.
When was CaP Spheres Pellet Pack approved by the FDA?
CaP Spheres Pellet Pack received FDA 510(k) clearance on 2021-05-04, under approval number K203218.
What company makes CaP Spheres Pellet Pack?
CaP Spheres Pellet Pack is manufactured by Zimmer Biomet Spine, Inc..
What is the FDA product code for CaP Spheres Pellet Pack?
The FDA product code for CaP Spheres Pellet Pack is MQV.
Other Devices by Zimmer Biomet Spine, Inc.
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.