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FDA 510(k)

PASS LP Spinal System

K-Number: K153413 · 2016-04-22

Decision Date2016-04-22
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PASS LP Spinal System is the device name listed in this FDA 510(k) record. The listed applicant is Medicrea International SA. It received FDA 510(k) clearance on 2016-04-22 under 510(k) number K153413. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PASS LP Spinal System?

PASS LP Spinal System is a medical device that received FDA 510(k) clearance on 2016-04-22. The listed applicant is Medicrea International SA. The 510(k) number is K153413.

When did PASS LP Spinal System receive FDA 510(k) clearance?

PASS LP Spinal System received FDA 510(k) clearance on 2016-04-22, under 510(k) number K153413.

Who is the listed applicant for PASS LP Spinal System?

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

What is the FDA product code for PASS LP Spinal System?

The FDA product code for PASS LP Spinal System is NKB.

Other records listing Medicrea International SA 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: NKB)

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.