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FDA 510(k)

POLY INSERT 20 DEGREE

K-Number: K920929 · 1993-05-05

ApplicantDow Corning Wright
Decision Date1993-05-05
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POLY INSERT 20 DEGREE is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1993-05-05 under 510(k) number K920929. 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 POLY INSERT 20 DEGREE?

POLY INSERT 20 DEGREE is a medical device that received FDA 510(k) clearance on 1993-05-05. The listed applicant is Dow Corning Wright. The 510(k) number is K920929.

When did POLY INSERT 20 DEGREE receive FDA 510(k) clearance?

POLY INSERT 20 DEGREE received FDA 510(k) clearance on 1993-05-05, under 510(k) number K920929.

Who is the listed applicant for POLY INSERT 20 DEGREE?

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

What is the FDA product code for POLY INSERT 20 DEGREE?

The FDA product code for POLY INSERT 20 DEGREE is JDL.

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Other records listing Dow Corning Wright 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.

K932210ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENTK932911ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENTK934354LACEY ALL POLYETHYLENE TIBIAL COMPONENTK932222SLT FEMORAL HEADK932858ORTHOLOC ADVANTIM TIBIAL BASE COMPONENTK930228ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE

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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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