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FDA 510(k)

HEMASORBPLUS Resorbable Hemostatic Bone Putty

K-Number: K153317 · 2016-11-30

ApplicantOrthocon, Inc.
Decision Date2016-11-30
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

HEMASORBPLUS Resorbable Hemostatic Bone Putty is a medical device manufactured by Orthocon, Inc.. It received FDA 510(k) clearance on 2016-11-30 under approval number K153317. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMASORBPLUS Resorbable Hemostatic Bone Putty?

HEMASORBPLUS Resorbable Hemostatic Bone Putty is a medical device that received FDA 510(k) clearance on 2016-11-30. It is manufactured by Orthocon, Inc.. The 510(k) number is K153317.

When was HEMASORBPLUS Resorbable Hemostatic Bone Putty approved by the FDA?

HEMASORBPLUS Resorbable Hemostatic Bone Putty received FDA 510(k) clearance on 2016-11-30, under approval number K153317.

What company makes HEMASORBPLUS Resorbable Hemostatic Bone Putty?

HEMASORBPLUS Resorbable Hemostatic Bone Putty is manufactured by Orthocon, Inc..

What is the FDA product code for HEMASORBPLUS Resorbable Hemostatic Bone Putty?

The FDA product code for HEMASORBPLUS Resorbable Hemostatic Bone Putty is MTJ.

Other Devices by Orthocon, Inc.

K191140MONTAGE-QS Settable, Resorbable Hemostatic Bone K193052HBP6 Settable, Resorbable Hemostatic Bone Paste K202363HBP7 Settable Hemostatic Bone Putty K220315MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty K231475MONTAGE-QS Settable, Resorbable Bone Putty K232998Montage- XT Settable, Resorbable Hemostatic Bone Putty

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Related Devices (Code: MTJ)

K153095ROP Resorbable Hemostasis MaterialResorbable Orthopedic Products, LLC K191140MONTAGE-QS Settable, Resorbable Hemostatic BoneOrthocon, Inc. K193052HBP6 Settable, Resorbable Hemostatic Bone PasteOrthocon, Inc. K202363HBP7 Settable Hemostatic Bone PuttyOrthocon, Inc. K220315MONTAGE-XT Settable, Resorbable Hemostatic Bone PuttyOrthocon, Inc. K232998Montage- XT Settable, Resorbable Hemostatic Bone PuttyOrthocon, Inc.

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.

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