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FDA 510(k)

HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX

K-Number: K111575 · 2012-05-23

Decision Date2012-05-23
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2012-05-23 under 510(k) number K111575. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX?

HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX is a medical device that received FDA 510(k) clearance on 2012-05-23. The listed applicant is Orthocon, Inc.. The 510(k) number is K111575.

When did HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX receive FDA 510(k) clearance?

HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX received FDA 510(k) clearance on 2012-05-23, under 510(k) number K111575.

Who is the listed applicant for HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX?

The FDA 510(k) record lists Orthocon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX?

The FDA product code for HEMASORB ABSORBABLE BONE HEMOSTAT MATRIX is MTJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Orthocon, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 33 devices →

Related Devices (Code: MTJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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