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FDA 510(k)

SILASTIC NASAL IMPLANT S-TYPE

K-Number: K880405 · 1988-02-18

ApplicantDow Corning Wright
Decision Date1988-02-18
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SILASTIC NASAL IMPLANT S-TYPE 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 1988-02-18 under 510(k) number K880405. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC NASAL IMPLANT S-TYPE?

SILASTIC NASAL IMPLANT S-TYPE is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Dow Corning Wright. The 510(k) number is K880405.

When did SILASTIC NASAL IMPLANT S-TYPE receive FDA 510(k) clearance?

SILASTIC NASAL IMPLANT S-TYPE received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880405.

Who is the listed applicant for SILASTIC NASAL IMPLANT S-TYPE?

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 SILASTIC NASAL IMPLANT S-TYPE?

The FDA product code for SILASTIC NASAL IMPLANT S-TYPE is FZE.

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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: FZE)

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.

K241253Medicon Epiplating SystemCmf Medicon Surgical, Inc.K161548Osseointegrated FixturesSouthern Implants (Pty), Ltd.K090803HANSON MEDICAL FACIAL IMPLANTSHanson Medical, Inc.K090630NOBEL BIOCARE ENDOSSEOUS IMPLANTS (MAXILLOFACIAL INDICATION)Nobel Biocare ABK071018MONARCH NASAL IMPLANTHanson Medical, Inc.K041690MONARCH NASAL IMPLANTHanson Medical, 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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