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FDA 510(k)

GLADIATOR PLASMA CLASSIC HIP STEM

K-Number: K110399 · 2011-05-10

Decision Date2011-05-10
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GLADIATOR PLASMA CLASSIC HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2011-05-10 under 510(k) number K110399. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLADIATOR PLASMA CLASSIC HIP STEM?

GLADIATOR PLASMA CLASSIC HIP STEM is a medical device that received FDA 510(k) clearance on 2011-05-10. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K110399.

When did GLADIATOR PLASMA CLASSIC HIP STEM receive FDA 510(k) clearance?

GLADIATOR PLASMA CLASSIC HIP STEM received FDA 510(k) clearance on 2011-05-10, under 510(k) number K110399.

Who is the listed applicant for GLADIATOR PLASMA CLASSIC HIP STEM?

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 GLADIATOR PLASMA CLASSIC HIP STEM?

The FDA product code for GLADIATOR PLASMA CLASSIC HIP STEM is KWA.

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.

Other records listing Wrightmedicaltechnologyinc 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.

View all 268 devices →

Related Devices (Code: KWA)

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.

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.

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