510(k) K220315
K220315 is an FDA 510(k) premarket notification submitted by Orthocon, Inc. for the device "MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty". The FDA issued a decision of Substantially Equivalent on Mar 11, 2022. The device falls under product code MTJ (Wax, Bone), a Class U device. Orthocon, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 11, 2022
- Date Received
- Feb 3, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wax, Bone
- Device Class
- Class U
- Regulation Number
- Review Panel
- OR
- Submission Type