FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Permatage XT Settable Bone Putty

K Number: K261265 · Decision Jun 15, 2026
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
43
Applicant Total
36
Review Days
60

Basic Information

Device Name
Permatage XT Settable Bone Putty
K Number
K261265
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5300
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthocon, Inc.
Date Received
April 16, 2026
Decision Date
June 15, 2026
Product Code
GXP
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXP Methyl Methacrylate For Cranioplasty

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Other 510(k) clearances with the same product code (GXP), ordered by most recent decision date.

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Other Clearances by Orthocon, Inc.

K Number Device Name
K261439 Permatage Flowable, Settable Hemostatic Bone Paste
K253447 Montage Flowable Settable, Resorbable Bone Paste (Burr Hole Cover)
K253732 Permatage Flowable, Settable Bone Paste
K253854 MONTAGE XT Cranial Cement
K243526 MONTAGE Settable, Resorbable Bone Putty MONTAGE-QS Settable, Resorbable Bone Putty MONTAGE Flowable Settable, Resorbable Bone Paste MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty
K243506 Montage-XT Settable Bone Putty
K241027 Permatage Settable Bone Putty
K233566 Montage-XT Settable, Resorbable Bone Putty
K242050 Montage Settable Bone Putty
K232771 Montage Flowable Settable, Resorbable Bone Paste
Search all 36 clearances from Orthocon, Inc. →