510(k) K261265

Permatage XT Settable Bone Putty by Orthocon, Inc. — Product Code GXP

K261265 is an FDA 510(k) premarket notification submitted by Orthocon, Inc. for the device "Permatage XT Settable Bone Putty". The FDA issued a decision of Substantially Equivalent on June 15, 2026. The device falls under product code GXP (Methyl Methacrylate For Cranioplasty), a Class II device regulated under 21 CFR 882.5300. Orthocon, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 15, 2026
Date Received
April 16, 2026
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Methyl Methacrylate For Cranioplasty
Device Class
Class II
Regulation Number
882.5300
Review Panel
NE
Submission Type