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FDA 510(k)

CODMAN SURGICAL PATTIE

K-Number: K880402 · 1988-03-02

ApplicantCodman & Shurtleff, Inc.
Decision Date1988-03-02
Product CodeHBA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN SURGICAL PATTIE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1988-03-02 under 510(k) number K880402. The device is classified under product code HBA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN SURGICAL PATTIE?

CODMAN SURGICAL PATTIE is a medical device that received FDA 510(k) clearance on 1988-03-02. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K880402.

When did CODMAN SURGICAL PATTIE receive FDA 510(k) clearance?

CODMAN SURGICAL PATTIE received FDA 510(k) clearance on 1988-03-02, under 510(k) number K880402.

Who is the listed applicant for CODMAN SURGICAL PATTIE?

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

What is the FDA product code for CODMAN SURGICAL PATTIE?

The FDA product code for CODMAN SURGICAL PATTIE is HBA.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: HBA)

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.

K193346Codman Surgical Patties & StripsIntegra LifeSciences CorporationK112598AMERICAN SURGICAL COMPANY/ NEUROSURGICAL SPONGES (BRAND)American Surgical Company, LLCK121822DELICOTAmerican Surgical Company, LLCK073576NEUROSURGICAL SPONGES AND PADDLES AND NEURO PATTIES AND NEUROSPONGESHarod Enterprises, Inc.K062406AESCULAP NEURO PATTIESAesculap, Inc.K031008AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)Aesculap

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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