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FDA 510(k)

KAMBIN SPINAL INSTRUMENT SET

K-Number: K853678 · 1985-09-24

ApplicantPilling Co.
Decision Date1985-09-24
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KAMBIN SPINAL INSTRUMENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1985-09-24 under 510(k) number K853678. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAMBIN SPINAL INSTRUMENT SET?

KAMBIN SPINAL INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 1985-09-24. The listed applicant is Pilling Co.. The 510(k) number is K853678.

When did KAMBIN SPINAL INSTRUMENT SET receive FDA 510(k) clearance?

KAMBIN SPINAL INSTRUMENT SET received FDA 510(k) clearance on 1985-09-24, under 510(k) number K853678.

Who is the listed applicant for KAMBIN SPINAL INSTRUMENT SET?

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

What is the FDA product code for KAMBIN SPINAL INSTRUMENT SET?

The FDA product code for KAMBIN SPINAL INSTRUMENT SET is HTZ.

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Other records listing Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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Related Devices (Code: HTZ)

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.

K933933CEBOPLANESynvasive Technology, Inc.K931737HEDLEYL INTRAMEDULLARY PREPARATION BRUSHSynvasive Technology, Inc.K87088245 DEGREE SHAVERBowen & Company, Inc.K850527ARTHROSCOPY SUCTION BIOPSY PUNCHT. Korossurgical Instruments Corp.K850423CONCEPT SUCTION SLEEVEConcept, Inc.K841980SIDE CUTTING SERRATED BLADEStainless Mfg., Inc.

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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