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FDA 510(k)

VERSYS HIP SYSTEM BEADED HIP PROSTHESIS

K-Number: K973714 · 1997-12-24

ApplicantZimmer, Inc.
Decision Date1997-12-24
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERSYS HIP SYSTEM BEADED HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1997-12-24 under 510(k) number K973714. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERSYS HIP SYSTEM BEADED HIP PROSTHESIS?

VERSYS HIP SYSTEM BEADED HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1997-12-24. The listed applicant is Zimmer, Inc.. The 510(k) number is K973714.

When did VERSYS HIP SYSTEM BEADED HIP PROSTHESIS receive FDA 510(k) clearance?

VERSYS HIP SYSTEM BEADED HIP PROSTHESIS received FDA 510(k) clearance on 1997-12-24, under 510(k) number K973714.

Who is the listed applicant for VERSYS HIP SYSTEM BEADED HIP PROSTHESIS?

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 VERSYS HIP SYSTEM BEADED HIP PROSTHESIS?

The FDA product code for VERSYS HIP SYSTEM BEADED HIP PROSTHESIS is LPH.

Related Clinical Trials

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.

Other records listing Zimmer, Inc. as applicant

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.

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Related Devices (Code: LPH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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