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FDA 510(k)

SPINAL CONCEPTS INC. PATHFINDER

K-Number: K030625 · 2003-03-28

ApplicantSpinal Concepts, Inc.
Decision Date2003-03-28
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SPINAL CONCEPTS INC. PATHFINDER is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Concepts, Inc.. It received FDA 510(k) clearance on 2003-03-28 under 510(k) number K030625. 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 SPINAL CONCEPTS INC. PATHFINDER?

SPINAL CONCEPTS INC. PATHFINDER is a medical device that received FDA 510(k) clearance on 2003-03-28. The listed applicant is Spinal Concepts, Inc.. The 510(k) number is K030625.

When did SPINAL CONCEPTS INC. PATHFINDER receive FDA 510(k) clearance?

SPINAL CONCEPTS INC. PATHFINDER received FDA 510(k) clearance on 2003-03-28, under 510(k) number K030625.

Who is the listed applicant for SPINAL CONCEPTS INC. PATHFINDER?

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

What is the FDA product code for SPINAL CONCEPTS INC. PATHFINDER?

The FDA product code for SPINAL CONCEPTS INC. PATHFINDER is NKB.

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Other records listing Spinal Concepts, Inc. as applicant

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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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