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FDA 510(k)

MTF ALLOGRAFT ANCHOR

K-Number: K042038 · 2004-12-23

ApplicantMusculoskeletal Transplant Foundation
Decision Date2004-12-23
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MTF ALLOGRAFT ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Musculoskeletal Transplant Foundation. It received FDA 510(k) clearance on 2004-12-23 under 510(k) number K042038. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTF ALLOGRAFT ANCHOR?

MTF ALLOGRAFT ANCHOR is a medical device that received FDA 510(k) clearance on 2004-12-23. The listed applicant is Musculoskeletal Transplant Foundation. The 510(k) number is K042038.

When did MTF ALLOGRAFT ANCHOR receive FDA 510(k) clearance?

MTF ALLOGRAFT ANCHOR received FDA 510(k) clearance on 2004-12-23, under 510(k) number K042038.

Who is the listed applicant for MTF ALLOGRAFT ANCHOR?

The FDA 510(k) record lists Musculoskeletal Transplant Foundation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTF ALLOGRAFT ANCHOR?

The FDA product code for MTF ALLOGRAFT ANCHOR is GAT.

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Other records listing Musculoskeletal Transplant Foundation as applicant

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Related Devices (Code: GAT)

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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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