FDA 510(k)

INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP

K-Number: K983942 · 1998-12-04

Decision Date1998-12-04

Product CodeJDS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1998-12-04 under 510(k) number K983942. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP?

INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP is a medical device that received FDA 510(k) clearance on 1998-12-04. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K983942.

When did INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP receive FDA 510(k) clearance?

INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP received FDA 510(k) clearance on 1998-12-04, under 510(k) number K983942.

Who is the listed applicant for INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP?

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

What is the FDA product code for INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP?

The FDA product code for INTRAMEDULLARY NAIL SYSTEM, LOCKING SCREW, NAIL CAP is JDS.

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Related Devices (Code: JDS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.