Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

2710-000 OSCILLATING SAW, GENERAL ASSEMBLY

K-Number: K905383 · 1991-06-18

ApplicantMicro Surgical Instruments Corp.
Decision Date1991-06-18
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

2710-000 OSCILLATING SAW, GENERAL ASSEMBLY 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 1991-06-18 under 510(k) number K905383. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY?

2710-000 OSCILLATING SAW, GENERAL ASSEMBLY is a medical device that received FDA 510(k) clearance on 1991-06-18. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K905383.

When did 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY receive FDA 510(k) clearance?

2710-000 OSCILLATING SAW, GENERAL ASSEMBLY received FDA 510(k) clearance on 1991-06-18, under 510(k) number K905383.

Who is the listed applicant for 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY?

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 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY?

The FDA product code for 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY is GEY.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 SYSTEMK915139MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULEK914346DRILL MODULES MODELS 2116/2117

View all 15 devices →

Related Devices (Code: GEY)

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., 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.

↑