Cleared Traditional

HBP7 Settable Hemostatic Bone Putty

K202363 · Orthocon, Inc. · General & Plastic Surgery
Jan 2021
Decision
153d
Days
Risk

About This 510(k) Submission

K202363 is an FDA 510(k) clearance for the HBP7 Settable Hemostatic Bone Putty, a Wax, Bone, submitted by Orthocon, Inc. (Irvington, US). The FDA issued a Cleared decision on January 19, 2021, 153 days after receiving the submission on August 19, 2020. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K202363 FDA.gov
FDA Decision Cleared SESE
Date Received August 19, 2020
Decision Date January 19, 2021
Days to Decision 153 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code MTJ — Wax, Bone
Device Class

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