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FDA 510(k)

DORR HIP PROSTHESIS, ACETABULAR COMPON

K-Number: K842893 · 1984-11-08

ApplicantCarbomedics, Inc.
Decision Date1984-11-08
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DORR HIP PROSTHESIS, ACETABULAR COMPON is the device name listed in this FDA 510(k) record. The listed applicant is Carbomedics, Inc.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K842893. 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 DORR HIP PROSTHESIS, ACETABULAR COMPON?

DORR HIP PROSTHESIS, ACETABULAR COMPON is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Carbomedics, Inc.. The 510(k) number is K842893.

When did DORR HIP PROSTHESIS, ACETABULAR COMPON receive FDA 510(k) clearance?

DORR HIP PROSTHESIS, ACETABULAR COMPON received FDA 510(k) clearance on 1984-11-08, under 510(k) number K842893.

Who is the listed applicant for DORR HIP PROSTHESIS, ACETABULAR COMPON?

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

What is the FDA product code for DORR HIP PROSTHESIS, ACETABULAR COMPON?

The FDA product code for DORR HIP PROSTHESIS, ACETABULAR COMPON is JDL.

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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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