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FDA 510(k)

CPS ACETABULAR COMPONENT

K-Number: K915527 · 1993-06-24

ApplicantImplantology Corp.
Decision Date1993-06-24
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CPS ACETABULAR COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Implantology Corp.. It received FDA 510(k) clearance on 1993-06-24 under 510(k) number K915527. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPS ACETABULAR COMPONENT?

CPS ACETABULAR COMPONENT is a medical device that received FDA 510(k) clearance on 1993-06-24. The listed applicant is Implantology Corp.. The 510(k) number is K915527.

When did CPS ACETABULAR COMPONENT receive FDA 510(k) clearance?

CPS ACETABULAR COMPONENT received FDA 510(k) clearance on 1993-06-24, under 510(k) number K915527.

Who is the listed applicant for CPS ACETABULAR COMPONENT?

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

What is the FDA product code for CPS ACETABULAR COMPONENT?

The FDA product code for CPS ACETABULAR COMPONENT is JDL.

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Other records listing Implantology Corp. 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.

K934729UFC HIP STEM COMPONENTS: HYDROXYLAPATITE COATEDK915529FPC/SFPC/RFPC ACETABULAR COMPONENTK915528BHR BIPOLAR FEMORAL HEAD COMPONENTK915385PPC HIP STEM COMPONENTK915391FPC HIP STEM COMPONENTK924099UFC HIP STEM COMPONENT

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Related Devices (Code: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, 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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