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FDA 510(k)

EXCIA

K-Number: K061699 · 2006-08-18

ApplicantAesculap, Inc.
Decision Date2006-08-18
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXCIA is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2006-08-18 under 510(k) number K061699. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXCIA?

EXCIA is a medical device that received FDA 510(k) clearance on 2006-08-18. The listed applicant is Aesculap, Inc.. The 510(k) number is K061699.

When did EXCIA receive FDA 510(k) clearance?

EXCIA received FDA 510(k) clearance on 2006-08-18, under 510(k) number K061699.

Who is the listed applicant for EXCIA?

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

What is the FDA product code for EXCIA?

The FDA product code for EXCIA is LWJ.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: LWJ)

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.

K120595UNISYN PLUS HIP STEMConsensus Orthopedics, Inc.K103518TRINITY ACETABULAR SYSTEMCorin USAK090764NOVATION CFS PRESS-FIT AND CEMENTED STEMSExactech, Inc.K082146METHA SHORT STEM HIP SYSTEM XL FEMORAL HEADAesculap Implant Systems, Inc.K07006136MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTHayes Medical, Inc.K062978U2 HIP STEM, TI PLASMA SPRAYUnited Orthopedic Corp.

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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