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FDA 510(k)

THERIGRAFT TCP PUTTY BONE VOID FILLER

K-Number: K053228 · 2006-01-31

ApplicantTherics, LLC
Decision Date2006-01-31
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THERIGRAFT TCP PUTTY BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Therics, LLC. It received FDA 510(k) clearance on 2006-01-31 under 510(k) number K053228. 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 THERIGRAFT TCP PUTTY BONE VOID FILLER?

THERIGRAFT TCP PUTTY BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2006-01-31. The listed applicant is Therics, LLC. The 510(k) number is K053228.

When did THERIGRAFT TCP PUTTY BONE VOID FILLER receive FDA 510(k) clearance?

THERIGRAFT TCP PUTTY BONE VOID FILLER received FDA 510(k) clearance on 2006-01-31, under 510(k) number K053228.

Who is the listed applicant for THERIGRAFT TCP PUTTY BONE VOID FILLER?

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

What is the FDA product code for THERIGRAFT TCP PUTTY BONE VOID FILLER?

The FDA product code for THERIGRAFT TCP PUTTY BONE VOID FILLER 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.

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.

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