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FDA 510(k)

FPC/SFPC/RFPC ACETABULAR COMPONENT

K-Number: K915529 · 1993-07-13

ApplicantImplantology Corp.
Decision Date1993-07-13
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FPC/SFPC/RFPC 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 1993-07-13 under 510(k) number K915529. 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 FPC/SFPC/RFPC ACETABULAR COMPONENT?

FPC/SFPC/RFPC ACETABULAR COMPONENT is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Implantology Corp.. The 510(k) number is K915529.

When did FPC/SFPC/RFPC ACETABULAR COMPONENT receive FDA 510(k) clearance?

FPC/SFPC/RFPC ACETABULAR COMPONENT received FDA 510(k) clearance on 1993-07-13, under 510(k) number K915529.

Who is the listed applicant for FPC/SFPC/RFPC 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 FPC/SFPC/RFPC ACETABULAR COMPONENT?

The FDA product code for FPC/SFPC/RFPC ACETABULAR COMPONENT is JDL.

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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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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 COATEDK915528BHR BIPOLAR FEMORAL HEAD COMPONENTK915527CPS ACETABULAR 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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