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FDA 510(k)

ALLOFIX ANCHOR, 5.0 MM ANCHOR

K-Number: K061498 · 2006-07-06

ApplicantMusculoskeletal Transplant Foundation
Decision Date2006-07-06
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALLOFIX ANCHOR, 5.0 MM 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 2006-07-06 under 510(k) number K061498. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLOFIX ANCHOR, 5.0 MM ANCHOR?

ALLOFIX ANCHOR, 5.0 MM ANCHOR is a medical device that received FDA 510(k) clearance on 2006-07-06. The listed applicant is Musculoskeletal Transplant Foundation. The 510(k) number is K061498.

When did ALLOFIX ANCHOR, 5.0 MM ANCHOR receive FDA 510(k) clearance?

ALLOFIX ANCHOR, 5.0 MM ANCHOR received FDA 510(k) clearance on 2006-07-06, under 510(k) number K061498.

Who is the listed applicant for ALLOFIX ANCHOR, 5.0 MM 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 ALLOFIX ANCHOR, 5.0 MM ANCHOR?

The FDA product code for ALLOFIX ANCHOR, 5.0 MM ANCHOR is JDW.

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Related Devices (Code: JDW)

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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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