Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM

K-Number: K111699 · 2011-08-19

Decision Date2011-08-19
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROFEMUR(R) Z TITANIUM PLASMA SPRAYED 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 2011-08-19 under 510(k) number K111699. 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 PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM?

PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM is a medical device that received FDA 510(k) clearance on 2011-08-19. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K111699.

When did PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM receive FDA 510(k) clearance?

PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM received FDA 510(k) clearance on 2011-08-19, under 510(k) number K111699.

Who is the listed applicant for PROFEMUR(R) Z TITANIUM PLASMA SPRAYED 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 PROFEMUR(R) Z TITANIUM PLASMA SPRAYED HIP STEM?

The FDA product code for PROFEMUR(R) Z TITANIUM PLASMA SPRAYED 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

View on FDA Database →

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

↑