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FDA 510(k)

Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)

K-Number: K262769 · 2026-09-03

Decision Date2026-09-03
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) is the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2026-09-03 under 510(k) number K262769. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)?

Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) is a medical device that received FDA 510(k) clearance on 2026-09-03. The listed applicant is Orthocon, Inc.. The 510(k) number is K262769.

When did Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) receive FDA 510(k) clearance?

Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) received FDA 510(k) clearance on 2026-09-03, under 510(k) number K262769.

Who is the listed applicant for Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)?

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 XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)?

The FDA product code for Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) 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.

View all 25 devices →

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.