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FDA 510(k)

CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)

K-Number: K982390 · 1998-09-14

ApplicantWrightmedicaltechnologyinc
Decision Date1998-09-14
Product CodeKTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1998-09-14 under 510(k) number K982390. The device is classified under product code KTW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)?

CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) is a medical device that received FDA 510(k) clearance on 1998-09-14. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K982390.

When did CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) receive FDA 510(k) clearance?

CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) received FDA 510(k) clearance on 1998-09-14, under 510(k) number K982390.

Who is the listed applicant for CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)?

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

What is the FDA product code for CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE)?

The FDA product code for CONCISE COMPRESSION HIP SCREW SYSTEM (STERILE) is KTW.

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Related Devices (Code: KTW)

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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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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