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FDA 510(k)

BONE RONGEUR, SINGLE-ACTION

K-Number: K890255 · 1989-01-27

ApplicantKinetic Medical Products
Decision Date1989-01-27
Product CodeEMH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BONE RONGEUR, SINGLE-ACTION is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Medical Products. It received FDA 510(k) clearance on 1989-01-27 under 510(k) number K890255. The device is classified under product code EMH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE RONGEUR, SINGLE-ACTION?

BONE RONGEUR, SINGLE-ACTION is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Kinetic Medical Products. The 510(k) number is K890255.

When did BONE RONGEUR, SINGLE-ACTION receive FDA 510(k) clearance?

BONE RONGEUR, SINGLE-ACTION received FDA 510(k) clearance on 1989-01-27, under 510(k) number K890255.

Who is the listed applicant for BONE RONGEUR, SINGLE-ACTION?

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

What is the FDA product code for BONE RONGEUR, SINGLE-ACTION?

The FDA product code for BONE RONGEUR, SINGLE-ACTION is EMH.

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Other records listing Kinetic Medical Products 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.

K890385MIDWIFERY/OBSTETRICAL FORCEPSK890380CERVICAL BIOPSY FORCEPSK890387MALLEABLE PLACENTA CURETTEK890382COMPRESSION FORCEPSK890376VAGINAL SPECULUMK890383HYSTERECTOMY FORCEPS

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Related Devices (Code: EMH)

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.

K890256BONE RONGEUR, DOUBLE-ACTIONKinetic Medical ProductsK854887MANU/SURG INST/ACCESS WUERZBURG TIT MINI BONE PLATWalter Lorenz Surgical, Inc.K851710586 TO 596 VARIOUS TYPES DENTAL ROOT SPLINTER FORCArtiberiaK834190JAKOBI SURG. INSTRUMENTS #8 15Imm Enterprises , Ltd.K834366SURGICAL INSTRUMENTS & ACCESSORIESC.B.S. Biotechnics, Inc.K821358MODIFIED RONGEURS FOR SPINAL & ORTH. S.Downs Surgical , Ltd.

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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