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FDA 510(k)

PACIFIC SURGICAL PATTIES

K-Number: K993019 · 2000-03-30

Decision Date2000-03-30
Product CodeHBA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PACIFIC SURGICAL PATTIES is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller Neuro/Spine. It received FDA 510(k) clearance on 2000-03-30 under 510(k) number K993019. The device is classified under product code HBA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACIFIC SURGICAL PATTIES?

PACIFIC SURGICAL PATTIES is a medical device that received FDA 510(k) clearance on 2000-03-30. The listed applicant is V. Mueller Neuro/Spine. The 510(k) number is K993019.

When did PACIFIC SURGICAL PATTIES receive FDA 510(k) clearance?

PACIFIC SURGICAL PATTIES received FDA 510(k) clearance on 2000-03-30, under 510(k) number K993019.

Who is the listed applicant for PACIFIC SURGICAL PATTIES?

The FDA 510(k) record lists V. Mueller Neuro/Spine as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PACIFIC SURGICAL PATTIES?

The FDA product code for PACIFIC SURGICAL PATTIES is HBA.

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 V. Mueller Neuro/Spine 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 8 devices →

Related Devices (Code: HBA)

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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