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FDA 510(k)

CEBOPLANE

K-Number: K933933 · 1994-04-15

ApplicantSynvasive Technology, Inc.
Decision Date1994-04-15
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CEBOPLANE is the device name listed in this FDA 510(k) record. The listed applicant is Synvasive Technology, Inc.. It received FDA 510(k) clearance on 1994-04-15 under 510(k) number K933933. 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 CEBOPLANE?

CEBOPLANE is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Synvasive Technology, Inc.. The 510(k) number is K933933.

When did CEBOPLANE receive FDA 510(k) clearance?

CEBOPLANE received FDA 510(k) clearance on 1994-04-15, under 510(k) number K933933.

Who is the listed applicant for CEBOPLANE?

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

What is the FDA product code for CEBOPLANE?

The FDA product code for CEBOPLANE is HTZ.

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Other records listing Synvasive Technology, Inc. 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.

K093046ELIBRA UNI SOFT-TISSUE FORCE SENSOR, MODEL 61-XXXX(5 MODELS, DIFFERENT SIZESK070108ELIBRA DYNAMIC KNEE BALANCERK972508SURGICAL BURS AND SURGICAL DRILL BITSK961522KIRSCHNER WIRE (K-WIRE) AND STEINMANN PINK950009POWERGRIP(TM) COMPRESSION FIXATION DEVICEK934336SPINALPLANE

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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.

K931737HEDLEYL INTRAMEDULLARY PREPARATION BRUSHSynvasive Technology, Inc.K87088245 DEGREE SHAVERBowen & Company, Inc.K853678KAMBIN SPINAL INSTRUMENT SETPilling Co.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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