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FDA 510(k)

SNT DISPOSABLE BIOPSY NEEDLE

K-Number: K971247 · 1997-06-16

Decision Date1997-06-16
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SNT DISPOSABLE BIOPSY NEEDLE 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 1997-06-16 under 510(k) number K971247. 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 SNT DISPOSABLE BIOPSY NEEDLE?

SNT DISPOSABLE BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1997-06-16. The listed applicant is Surgical Navigation Technologies, Inc.. The 510(k) number is K971247.

When did SNT DISPOSABLE BIOPSY NEEDLE receive FDA 510(k) clearance?

SNT DISPOSABLE BIOPSY NEEDLE received FDA 510(k) clearance on 1997-06-16, under 510(k) number K971247.

Who is the listed applicant for SNT DISPOSABLE BIOPSY NEEDLE?

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 SNT DISPOSABLE BIOPSY NEEDLE?

The FDA product code for SNT DISPOSABLE BIOPSY NEEDLE is HAW.

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: HAW)

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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