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FDA 510(k)

QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM

K-Number: K964444 · 1997-08-11

ApplicantRdh Medical
Decision Date1997-08-11
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rdh Medical. It received FDA 510(k) clearance on 1997-08-11 under 510(k) number K964444. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM?

QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM is a medical device that received FDA 510(k) clearance on 1997-08-11. The listed applicant is Rdh Medical. The 510(k) number is K964444.

When did QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM receive FDA 510(k) clearance?

QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM received FDA 510(k) clearance on 1997-08-11, under 510(k) number K964444.

Who is the listed applicant for QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM?

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

What is the FDA product code for QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM?

The FDA product code for QUICKLOCK ORTHOPAEDIC TARGETING SYSTEM is HSB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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