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)

ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE

K-Number: K071206 · 2007-05-31

Decision Date2007-05-31
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE is the device name listed in this FDA 510(k) record. The listed applicant is Apatech , Ltd.. It received FDA 510(k) clearance on 2007-05-31 under 510(k) number K071206. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE?

ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE is a medical device that received FDA 510(k) clearance on 2007-05-31. The listed applicant is Apatech , Ltd.. The 510(k) number is K071206.

When did ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE receive FDA 510(k) clearance?

ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE received FDA 510(k) clearance on 2007-05-31, under 510(k) number K071206.

Who is the listed applicant for ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE?

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

What is the FDA product code for ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE?

The FDA product code for ACTIFUSE ABX E-Z-FIL PUTTY BONE GRAFT SUBSTITUTE is MQV.

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 Apatech , Ltd. 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 8 devices →

Related Devices (Code: MQV)

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.

↑