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FDA 510(k)

MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT

K-Number: K871956 · 1987-06-23

ApplicantDowns Surgical , Ltd.
Decision Date1987-06-23
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K871956. 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 MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT?

MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K871956.

When did MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT receive FDA 510(k) clearance?

MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT received FDA 510(k) clearance on 1987-06-23, under 510(k) number K871956.

Who is the listed applicant for MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT?

The FDA product code for MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT is KWA.

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Other records listing Downs Surgical , Ltd. as applicant

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K903750ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-EK903747ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-UK903749ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-UK903748ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-VK900609SHEPPERD STRAIGHT AND CURVED NEEDLESK900616SHEPPERD CUTTING FORCEPS

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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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