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FDA 510(k)

DEPUY ROCKWOOD CLAVICLE PIN

K-Number: K991649 · 1999-07-14

ApplicantDepuy, Inc.
Decision Date1999-07-14
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY ROCKWOOD CLAVICLE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1999-07-14 under 510(k) number K991649. 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 DEPUY ROCKWOOD CLAVICLE PIN?

DEPUY ROCKWOOD CLAVICLE PIN is a medical device that received FDA 510(k) clearance on 1999-07-14. The listed applicant is Depuy, Inc.. The 510(k) number is K991649.

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

DEPUY ROCKWOOD CLAVICLE PIN received FDA 510(k) clearance on 1999-07-14, under 510(k) number K991649.

Who is the listed applicant for DEPUY ROCKWOOD CLAVICLE PIN?

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

What is the FDA product code for DEPUY ROCKWOOD CLAVICLE PIN?

The FDA product code for DEPUY ROCKWOOD CLAVICLE PIN is JDW.

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.

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Other records listing Depuy, Inc. as applicant

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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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