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FDA 510(k)

SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED

K-Number: K874939 · 1988-02-02

ApplicantKirschner Medical Corp.
Decision Date1988-02-02
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent for Some Indications

Device Summary

SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1988-02-02 under 510(k) number K874939. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED?

SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K874939.

When did SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED receive FDA 510(k) clearance?

SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED received FDA 510(k) clearance on 1988-02-02, under 510(k) number K874939.

Who is the listed applicant for SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED?

The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED?

The FDA product code for SCHURMAN/CARTER II HIP PROSTHESIS, POROUS COATED is DXQ.

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Other records listing Kirschner Medical 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.

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Related Devices (Code: DXQ)

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.

K254287Medline Reusable Blood Pressure CuffMedline Industries, LPK260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden CorporationK253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare CorporationK250765AViTA Arm Type Blood Pressure Monitor CuffAvita Corporation

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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