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FDA 510(k)

WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS

K-Number: K811119 · 1981-07-20

ApplicantAllo Pro Corp.
Decision Date1981-07-20
Product Code
DecisionSubstantially Equivalent

Device Summary

WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1981-07-20 under 510(k) number K811119. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS?

WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Allo Pro Corp.. The 510(k) number is K811119.

When did WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS receive FDA 510(k) clearance?

WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811119.

Who is the listed applicant for WEBER/STUEHMER HIP JOINT ENDOPROSTHESIS?

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

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Other records listing Allo Pro Corp. 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.

K901581GSB ELBOWK900425SURGICAL COTTON GLOVESK900392CENTERING PLUGK896669WEBER PERMALOCKK892644BIOLOX CERAMIC BALLK885049RS-CUP ACETABULAR PROSTHESIS

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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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