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FDA 510(k)

BAUMER MULLER HIP PROSTHESIS

K-Number: K003976 · 2001-03-19

ApplicantBaumer, S.A
Decision Date2001-03-19
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BAUMER MULLER HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Baumer, S.A. It received FDA 510(k) clearance on 2001-03-19 under 510(k) number K003976. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAUMER MULLER HIP PROSTHESIS?

BAUMER MULLER HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 2001-03-19. The listed applicant is Baumer, S.A. The 510(k) number is K003976.

When did BAUMER MULLER HIP PROSTHESIS receive FDA 510(k) clearance?

BAUMER MULLER HIP PROSTHESIS received FDA 510(k) clearance on 2001-03-19, under 510(k) number K003976.

Who is the listed applicant for BAUMER MULLER HIP PROSTHESIS?

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

What is the FDA product code for BAUMER MULLER HIP PROSTHESIS?

The FDA product code for BAUMER MULLER HIP PROSTHESIS is JDI.

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 Baumer, S.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.

Related Devices (Code: JDI)

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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