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FDA 510(k)

ZWEYMUELLER-SL HIP PROSTHESIS STEM

K-Number: K871453 · 1987-07-13

ApplicantAllo Pro Corp.
Decision Date1987-07-13
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZWEYMUELLER-SL HIP PROSTHESIS STEM 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 1987-07-13 under 510(k) number K871453. 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 ZWEYMUELLER-SL HIP PROSTHESIS STEM?

ZWEYMUELLER-SL HIP PROSTHESIS STEM is a medical device that received FDA 510(k) clearance on 1987-07-13. The listed applicant is Allo Pro Corp.. The 510(k) number is K871453.

When did ZWEYMUELLER-SL HIP PROSTHESIS STEM receive FDA 510(k) clearance?

ZWEYMUELLER-SL HIP PROSTHESIS STEM received FDA 510(k) clearance on 1987-07-13, under 510(k) number K871453.

Who is the listed applicant for ZWEYMUELLER-SL HIP PROSTHESIS STEM?

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

What is the FDA product code for ZWEYMUELLER-SL HIP PROSTHESIS STEM?

The FDA product code for ZWEYMUELLER-SL HIP PROSTHESIS STEM is KWA.

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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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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.

K122778PROFEMUR Z REVISION HIP STEMWrightmedicaltechnologyincK121544DYNASTY BIOFOAM SHELLWrightmedicaltechnologyincK113271METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONSBiomet Manufacturing, Inc.K113322CONSERVE THIN SHELLWrightmedicaltechnologyincK112080PRESERVE HIP STEMWrightmedicaltechnologyincK112150PROFEMUR GLADIATOR HA HIP STEMWrightmedicaltechnologyinc

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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