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FDA 510(k)

RINGLOC CONSTRAINED LINER

K-Number: K950202 · 1995-05-15

ApplicantBiomet, Inc.
Decision Date1995-05-15
Product CodeKWZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RINGLOC CONSTRAINED LINER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K950202. The device is classified under product code KWZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RINGLOC CONSTRAINED LINER?

RINGLOC CONSTRAINED LINER is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Biomet, Inc.. The 510(k) number is K950202.

When did RINGLOC CONSTRAINED LINER receive FDA 510(k) clearance?

RINGLOC CONSTRAINED LINER received FDA 510(k) clearance on 1995-05-15, under 510(k) number K950202.

Who is the listed applicant for RINGLOC CONSTRAINED LINER?

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

What is the FDA product code for RINGLOC CONSTRAINED LINER?

The FDA product code for RINGLOC CONSTRAINED LINER is KWZ.

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Other records listing Biomet, Inc. as applicant

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Related Devices (Code: KWZ)

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.

K241461Mpact Constrained LinerMedacta International S.A.K240639PINNACLETM Constrained Acetabular LinersDepuy Ireland UCK162641Smith & Nephew, Inc. R3™ Constrained LinerSmith & Nephew, Inc.K163497EXPRT™ Revision Hip System - EXPRT™ Hip Distal Stem, EXPRT™ Hip Standard Offset Proximal Body Implant, EXPRT™ Hip Lateral Offset Proximal Body Implant, EXPRT™ Hip Capture BoltEncore Medical L.P.K161610EXPRT Revision Hip SystemEncore Medical L.P.K122139SMITH & NEPHEW R3 CONSTRAINED LINERSSmith & Nephew, Inc.

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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