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FDA 510(k)

GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION

K-Number: K931991 · 1993-08-20

ApplicantNomos Corp.
Decision Date1993-08-20
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION is the device name listed in this FDA 510(k) record. The listed applicant is Nomos Corp.. It received FDA 510(k) clearance on 1993-08-20 under 510(k) number K931991. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION?

GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION is a medical device that received FDA 510(k) clearance on 1993-08-20. The listed applicant is Nomos Corp.. The 510(k) number is K931991.

When did GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION receive FDA 510(k) clearance?

GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION received FDA 510(k) clearance on 1993-08-20, under 510(k) number K931991.

Who is the listed applicant for GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION?

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

What is the FDA product code for GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION?

The FDA product code for GNOMOS STEREOTACTIC SYSTEM W/ NONINVASIVE FIXATION is HAW.

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Other records listing Nomos Corp. as applicant

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Related Devices (Code: HAW)

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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.

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