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FDA 510(k)

Cove Putty, OsteoCove Putty

K-Number: K242273 · 2024-09-25

ApplicantSeaSpine Orthopedics Corporation
Decision Date2024-09-25
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cove Putty, OsteoCove Putty is the device name listed in this FDA 510(k) record. The listed applicant is SeaSpine Orthopedics Corporation. It received FDA 510(k) clearance on 2024-09-25 under 510(k) number K242273. 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 2024-09-25. The listed applicant is SeaSpine Orthopedics Corporation. The 510(k) number is K242273.

When did Cove Putty, OsteoCove Putty receive FDA 510(k) clearance?

Cove Putty, OsteoCove Putty received FDA 510(k) clearance on 2024-09-25, under 510(k) number K242273.

Who is the listed applicant for Cove Putty, OsteoCove Putty?

The FDA 510(k) record lists SeaSpine Orthopedics Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

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