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FDA 510(k)

AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS

K-Number: K954652 · 1996-02-14

ApplicantAesculap, Inc.
Decision Date1996-02-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1996-02-14 under 510(k) number K954652. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS?

AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1996-02-14. The listed applicant is Aesculap, Inc.. The 510(k) number is K954652.

When did AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS receive FDA 510(k) clearance?

AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS received FDA 510(k) clearance on 1996-02-14, under 510(k) number K954652.

Who is the listed applicant for AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS?

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 AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS?

The FDA product code for AESCULAP ENDOSCCOPIC SPINE INSTRUMENTS is HRX.

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Related Devices (Code: HRX)

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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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