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FDA 510(k)

SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA

K-Number: K870843 · 1987-05-27

ApplicantWarsaw Orthopedic, Inc.
Decision Date1987-05-27
Product CodeHWT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA is the device name listed in this FDA 510(k) record. The listed applicant is Warsaw Orthopedic, Inc.. It received FDA 510(k) clearance on 1987-05-27 under 510(k) number K870843. The device is classified under product code HWT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA?

SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA is a medical device that received FDA 510(k) clearance on 1987-05-27. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K870843.

When did SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA receive FDA 510(k) clearance?

SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA received FDA 510(k) clearance on 1987-05-27, under 510(k) number K870843.

Who is the listed applicant for SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA?

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

What is the FDA product code for SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA?

The FDA product code for SCHULTZ PHALANGEAL COMP TRIAL/METACARPAL COMP TRIA is HWT.

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Other records listing Warsaw Orthopedic, Inc. as applicant

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K892877CRADLE, HOSPITAL BED CLOTHINGK883783TSRH SACRAL SPINAL SCREWK883784TSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATEK880211TSRH H/M HOOK HOLDERK880212TSRH H/M HOOK HOLDER W/ROD MOVERK880215TSRH H/M HOOK, EYEBOLT/LOCK NUT ASSEM., SPINAL ROD

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Related Devices (Code: HWT)

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.

K974406ORTHOPLANOrtho-Graphics, Inc.K960685ORTHODOC PREOPERATIVE PLANNER MODEL 500Integrated Surgical Systems, Inc.K894228KRONNER SPHERICAL CUTTERSKronner MedicalK871323ARTHROSCOPIC MENISCAL SUTURE SYSTEMOrthopedic Systems, Inc.K8303603M OSTEOTOMY GUIDE3M CompanyK811205MOLDED POLYSULFONE TRIAL PROSTHESISShannon Group

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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