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FDA 510(k)

INTRA-ARTICULATED ARTHRO POWER SYSTEM

K-Number: K871250 · 1987-04-27

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1987-04-27
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

INTRA-ARTICULATED ARTHRO POWER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1987-04-27 under 510(k) number K871250. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRA-ARTICULATED ARTHRO POWER SYSTEM?

INTRA-ARTICULATED ARTHRO POWER SYSTEM is a medical device that received FDA 510(k) clearance on 1987-04-27. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K871250.

When did INTRA-ARTICULATED ARTHRO POWER SYSTEM receive FDA 510(k) clearance?

INTRA-ARTICULATED ARTHRO POWER SYSTEM received FDA 510(k) clearance on 1987-04-27, under 510(k) number K871250.

Who is the listed applicant for INTRA-ARTICULATED ARTHRO POWER SYSTEM?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRA-ARTICULATED ARTHRO POWER SYSTEM?

The FDA product code for INTRA-ARTICULATED ARTHRO POWER SYSTEM is KIT.

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Other records listing Richard Wolf Medical Instruments Corp. as applicant

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Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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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