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FDA 510(k)

ROCKWOOD CLAVICLE PINS

K-Number: K103001 · 2011-02-17

ApplicantDePuy Orthopaedics, Inc.
Decision Date2011-02-17
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ROCKWOOD CLAVICLE PINS 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 2011-02-17 under 510(k) number K103001. 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 ROCKWOOD CLAVICLE PINS?

ROCKWOOD CLAVICLE PINS is a medical device that received FDA 510(k) clearance on 2011-02-17. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K103001.

When did ROCKWOOD CLAVICLE PINS receive FDA 510(k) clearance?

ROCKWOOD CLAVICLE PINS received FDA 510(k) clearance on 2011-02-17, under 510(k) number K103001.

Who is the listed applicant for ROCKWOOD CLAVICLE PINS?

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 ROCKWOOD CLAVICLE PINS?

The FDA product code for ROCKWOOD CLAVICLE PINS is 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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