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FDA 510(k)

MEMORY STAPLE

K-Number: K060746 · 2006-05-25

ApplicantDePuy Orthopaedics, Inc.
Decision Date2006-05-25
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEMORY STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2006-05-25 under 510(k) number K060746. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMORY STAPLE?

MEMORY STAPLE is a medical device that received FDA 510(k) clearance on 2006-05-25. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K060746.

When did MEMORY STAPLE receive FDA 510(k) clearance?

MEMORY STAPLE received FDA 510(k) clearance on 2006-05-25, under 510(k) number K060746.

Who is the listed applicant for MEMORY STAPLE?

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

What is the FDA product code for MEMORY STAPLE?

The FDA product code for MEMORY STAPLE is JDR.

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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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