FDA 510(k)

ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM

K-Number: K042783 · 2004-12-17

Decision Date2004-12-17

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 2004-12-17 under 510(k) number K042783. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM?

ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM is a medical device that received FDA 510(k) clearance on 2004-12-17. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K042783.

When did ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM receive FDA 510(k) clearance?

ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM received FDA 510(k) clearance on 2004-12-17, under 510(k) number K042783.

Who is the listed applicant for ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM?

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

What is the FDA product code for ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM?

The FDA product code for ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEM is HBE.

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Other records listing The Anspach Effort, 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.