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FDA 510(k)

RADIOCAMERAS EXTRACRANIAL SYSTEM

K-Number: K000246 · 2000-10-20

Decision Date2000-10-20
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOCAMERAS EXTRACRANIAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Navigation Technologies, Inc.. It received FDA 510(k) clearance on 2000-10-20 under 510(k) number K000246. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOCAMERAS EXTRACRANIAL SYSTEM?

RADIOCAMERAS EXTRACRANIAL SYSTEM is a medical device that received FDA 510(k) clearance on 2000-10-20. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K000246.

When did RADIOCAMERAS EXTRACRANIAL SYSTEM receive FDA 510(k) clearance?

RADIOCAMERAS EXTRACRANIAL SYSTEM received FDA 510(k) clearance on 2000-10-20, under 510(k) number K000246.

Who is the listed applicant for RADIOCAMERAS EXTRACRANIAL SYSTEM?

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

What is the FDA product code for RADIOCAMERAS EXTRACRANIAL SYSTEM?

The FDA product code for RADIOCAMERAS EXTRACRANIAL SYSTEM is IYE.

Related Clinical Trials

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.

Other records listing Surgical Navigation Technologies, Inc. as applicant

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.

View all 27 devices →

Related Devices (Code: IYE)

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.

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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