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FDA 510(k)

MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE

K-Number: K915139 · 1992-02-05

ApplicantMicro Surgical Instruments Corp.
Decision Date1992-02-05
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Micro Surgical Instruments Corp.. It received FDA 510(k) clearance on 1992-02-05 under 510(k) number K915139. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE?

MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE is a medical device that received FDA 510(k) clearance on 1992-02-05. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K915139.

When did MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE receive FDA 510(k) clearance?

MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE received FDA 510(k) clearance on 1992-02-05, under 510(k) number K915139.

Who is the listed applicant for MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE?

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

What is the FDA product code for MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE?

The FDA product code for MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULE is HSZ.

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Other records listing Micro Surgical Instruments Corp. 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.

K931395SERIES 5000 BATTERY POWERED INSTRUMENT SYSTEMK932492IMPLANTOLOGY MODULE, MODEL 2175K930205ELECTRIC WIRE DRIVER, MODEL 2640EK914998MICROAIRE(R) FACIAL BONE PLATING SYSTEMK914346DRILL MODULES MODELS 2116/2117K913369MICRO-AIRE MODEL 2060

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Related Devices (Code: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, 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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