Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY

K-Number: K122156 · 2013-01-28

Decision Date2013-01-28
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY is the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2013-01-28 under 510(k) number K122156. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY?

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY is a medical device that received FDA 510(k) clearance on 2013-01-28. The listed applicant is Orthocon, Inc.. The 510(k) number is K122156.

When did ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY receive FDA 510(k) clearance?

ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY received FDA 510(k) clearance on 2013-01-28, under 510(k) number K122156.

Who is the listed applicant for ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY?

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 ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY?

The FDA product code for ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY 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

View on FDA Database →

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

↑