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FDA 510(k)

ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS

K-Number: K033011 · 2004-02-12

ApplicantZimmer, Inc.
Decision Date2004-02-12
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2004-02-12 under 510(k) number K033011. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS?

ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2004-02-12. The listed applicant is Zimmer, Inc.. The 510(k) number is K033011.

When did ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS receive FDA 510(k) clearance?

ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS received FDA 510(k) clearance on 2004-02-12, under 510(k) number K033011.

Who is the listed applicant for ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS?

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

What is the FDA product code for ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS?

The FDA product code for ZIMMER ORTHO GUIDANCE SYSTEMS- KNEE INSTRUMENTS is HAW.

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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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