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FDA 510(k)

ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002

K-Number: K903213 · 1990-07-27

ApplicantPercutaneous Technologies
Decision Date1990-07-27
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 is the device name listed in this FDA 510(k) record. The listed applicant is Percutaneous Technologies. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K903213. The device is classified under product code HEX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002?

ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Percutaneous Technologies. The 510(k) number is K903213.

When did ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 receive FDA 510(k) clearance?

ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 received FDA 510(k) clearance on 1990-07-27, under 510(k) number K903213.

Who is the listed applicant for ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002?

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

What is the FDA product code for ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002?

The FDA product code for ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 is HEX.

Related Clinical Trials

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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Other records listing Percutaneous Technologies 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.

K904479SURGICAL INST.:1030,1010,1011,1012,1013,1014,1015

Related Devices (Code: HEX)

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.

K233043Smart Scope® CXPeriwinkle Technologies Pvt., Ltd.K190187Gynescope SystemIllumigyn , Ltd.K182764Biop Digital ColposcopeBiop Medical , Ltd.K181034Pocket Colposcope SystemHadleigh Health Technologies, LLCK170446LT-300 SD Digital Video ColposcopeLutech Industries, Inc.K161871EVA (Enhanced Visual Assessment) SystemMobileodt , Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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