Cove Putty, OsteoCove Putty
K-Number: K231030 · 2023-09-14
ApplicantSeaSpine Orthopedics Corporation
Decision Date2023-09-14
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Cove Putty, OsteoCove Putty is a medical device manufactured by SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2023-09-14 under approval number K231030. 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 Cove Putty, OsteoCove Putty?
Cove Putty, OsteoCove Putty is a medical device that received FDA 510(k) clearance on 2023-09-14. It is manufactured by SeaSpine Orthopedics Corporation. The 510(k) number is K231030.
When was Cove Putty, OsteoCove Putty approved by the FDA?
Cove Putty, OsteoCove Putty received FDA 510(k) clearance on 2023-09-14, under approval number K231030.
What company makes Cove Putty, OsteoCove Putty?
Cove Putty, OsteoCove Putty is manufactured by SeaSpine Orthopedics Corporation.
What is the FDA product code for Cove Putty, OsteoCove Putty?
The FDA product code for Cove Putty, OsteoCove Putty is MQV.
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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.