Permatage Flowable, Settable Hemostatic Bone Paste
K-Number: K261439 · 2026-06-03
Device Summary
Frequently Asked Questions
What is the Permatage Flowable, Settable Hemostatic Bone Paste?
Permatage Flowable, Settable Hemostatic Bone Paste is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Orthocon, Inc.. The 510(k) number is K261439.
When did Permatage Flowable, Settable Hemostatic Bone Paste receive FDA 510(k) clearance?
Permatage Flowable, Settable Hemostatic Bone Paste received FDA 510(k) clearance on 2026-06-03, under 510(k) number K261439.
Who is the listed applicant for Permatage Flowable, Settable Hemostatic Bone Paste?
The FDA 510(k) record lists Orthocon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Permatage Flowable, Settable Hemostatic Bone Paste?
The FDA product code for Permatage Flowable, Settable Hemostatic Bone Paste is MTJ.
Other records listing Orthocon, 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: MTJ)
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.