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FDA 510(k)

AOR X-RAY ALIGMENT PAD

K-Number: K837776 · 1983-08-18

ApplicantZimmer, Inc.
Decision Date1983-08-18
Product CodeIXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AOR X-RAY ALIGMENT PAD is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1983-08-18 under 510(k) number K837776. The device is classified under product code IXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOR X-RAY ALIGMENT PAD?

AOR X-RAY ALIGMENT PAD is a medical device that received FDA 510(k) clearance on 1983-08-18. The listed applicant is Zimmer, Inc.. The 510(k) number is K837776.

When did AOR X-RAY ALIGMENT PAD receive FDA 510(k) clearance?

AOR X-RAY ALIGMENT PAD received FDA 510(k) clearance on 1983-08-18, under 510(k) number K837776.

Who is the listed applicant for AOR X-RAY ALIGMENT PAD?

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

What is the FDA product code for AOR X-RAY ALIGMENT PAD?

The FDA product code for AOR X-RAY ALIGMENT PAD is IXJ.

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Related Devices (Code: IXJ)

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.

K964025MITAYA ALUMINUM INTERSPACED X-RAY GRIDX-Ray Accessory Corp.K963893FIBRE INTERSPACED X-RAY GRIDSmit RontgenK962338RADIOGRAPHIC GRIDUnidex Group, Inc.K954294HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZESThermotrex Corp.K945697SK S-RAY GRIDSSeibu Techno CoprorationK945327JPI X-RAY GRIDJpi America, Inc.

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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