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FDA 510(k)

FASCIA CUTTER

K-Number: K834514 · 1984-03-12

ApplicantStryker Corp.
Decision Date1984-03-12
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FASCIA CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K834514. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FASCIA CUTTER?

FASCIA CUTTER is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Stryker Corp.. The 510(k) number is K834514.

When did FASCIA CUTTER receive FDA 510(k) clearance?

FASCIA CUTTER received FDA 510(k) clearance on 1984-03-12, under 510(k) number K834514.

Who is the listed applicant for FASCIA CUTTER?

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

What is the FDA product code for FASCIA CUTTER?

The FDA product code for FASCIA CUTTER is GES.

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Other records listing Stryker 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

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Related Devices (Code: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K932998EASY-ONDevon Industries, Inc.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK900266STERILE CARBON STEEL SURGICAL BLADERahn Laboratories

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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