Moldable Bone Void Filler and Moldable Bone Void Filler + CCC
K-Number: K241555 · 2025-02-21
Device Summary
Frequently Asked Questions
What is the Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?
Moldable Bone Void Filler and Moldable Bone Void Filler + CCC is a medical device that received FDA 510(k) clearance on 2025-02-21. The listed applicant is Rti Surgical, Inc.. The 510(k) number is K241555.
When did Moldable Bone Void Filler and Moldable Bone Void Filler + CCC receive FDA 510(k) clearance?
Moldable Bone Void Filler and Moldable Bone Void Filler + CCC received FDA 510(k) clearance on 2025-02-21, under 510(k) number K241555.
Who is the listed applicant for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?
The FDA 510(k) record lists Rti Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?
The FDA product code for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC is MQV.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Rti Surgical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQV)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.