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FDA 510(k)

SPACER-G TEMPORARY HIP PROSTHESIS

K-Number: K062273 · 2008-05-22

ApplicantTecres S.P.A.
Decision Date2008-05-22
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPACER-G TEMPORARY HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Tecres S.P.A.. It received FDA 510(k) clearance on 2008-05-22 under 510(k) number K062273. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPACER-G TEMPORARY HIP PROSTHESIS?

SPACER-G TEMPORARY HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 2008-05-22. The listed applicant is Tecres S.P.A.. The 510(k) number is K062273.

When did SPACER-G TEMPORARY HIP PROSTHESIS receive FDA 510(k) clearance?

SPACER-G TEMPORARY HIP PROSTHESIS received FDA 510(k) clearance on 2008-05-22, under 510(k) number K062273.

Who is the listed applicant for SPACER-G TEMPORARY HIP PROSTHESIS?

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

What is the FDA product code for SPACER-G TEMPORARY HIP PROSTHESIS?

The FDA product code for SPACER-G TEMPORARY HIP PROSTHESIS is KWL.

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 Tecres S.P.A. 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.

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Related Devices (Code: KWL)

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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