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FDA 510(k)

820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS

K-Number: K851714 · 1985-06-11

ApplicantArtiberia
Decision Date1985-06-11
Product CodeEMM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K851714. The device is classified under product code EMM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS?

820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Artiberia. The 510(k) number is K851714.

When did 820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS receive FDA 510(k) clearance?

820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851714.

Who is the listed applicant for 820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS?

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

What is the FDA product code for 820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS?

The FDA product code for 820/1 TO 820/51 VARIOUS TYPES BONE RONGEURS is EMM.

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Other records listing Artiberia 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.

K8517451-100 UNIVERSAL SET OTOSCOPE & LARYNX EXPLORATON BK85178627-230 TO 27-234 VARIOUS CAST BREAKERS, WOLFK8517191070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERSK8517272020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CAK851718930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTESK8517201155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORS

View all 79 devices →

Related Devices (Code: EMM)

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.

K963897STERI-OSS SINUS AUGMENTATION KITSteri-Oss, Inc.K864775CHISEL (OSTEOTOME, GOUGE, ETC.)New England Surgical Instrument Corp.K760959SURGICAL CHISELAmerican Safety Equipment Corp.

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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