FDA 510(k)

INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS)

K-Number: K994363 · 2000-03-06

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date2000-03-06

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS) 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 2000-03-06 under 510(k) number K994363. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS)?

INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS) is a medical device that received FDA 510(k) clearance on 2000-03-06. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K994363.

When did INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS) receive FDA 510(k) clearance?

INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS) received FDA 510(k) clearance on 2000-03-06, under 510(k) number K994363.

Who is the listed applicant for INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS)?

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 INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS)?

The FDA product code for INSTRUMENTS FOR MINIMALLY INVASIVE SPINAL SURGERY (MISS) is HRX.

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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.