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FDA 510(k)

AESCULAP CESPACE XP

K-Number: K123909 · 2013-04-15

ApplicantAesculap Implant System, Inc.
Decision Date2013-04-15
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AESCULAP CESPACE XP is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Implant System, Inc.. It received FDA 510(k) clearance on 2013-04-15 under 510(k) number K123909. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP CESPACE XP?

AESCULAP CESPACE XP is a medical device that received FDA 510(k) clearance on 2013-04-15. The listed applicant is Aesculap Implant System, Inc.. The 510(k) number is K123909.

When did AESCULAP CESPACE XP receive FDA 510(k) clearance?

AESCULAP CESPACE XP received FDA 510(k) clearance on 2013-04-15, under 510(k) number K123909.

Who is the listed applicant for AESCULAP CESPACE XP?

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

What is the FDA product code for AESCULAP CESPACE XP?

The FDA product code for AESCULAP CESPACE XP is ODP.

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Other records listing Aesculap Implant System, Inc. as applicant

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Related Devices (Code: ODP)

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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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