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FDA 510(k)

PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP

K-Number: K991002 · 1999-06-11

Decision Date1999-06-11
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP 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 1999-06-11 under 510(k) number K991002. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP?

PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP is a medical device that received FDA 510(k) clearance on 1999-06-11. The listed applicant is V. Mueller Neuro/Spine. The 510(k) number is K991002.

When did PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP receive FDA 510(k) clearance?

PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP received FDA 510(k) clearance on 1999-06-11, under 510(k) number K991002.

Who is the listed applicant for PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP?

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 PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP?

The FDA product code for PSI TITANIUM MICRO-LIGATION HEMOSTATIC CLIP is FZP.

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: FZP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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