Model 2250-000 Zimmer Style Sagittal Saw Module

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K915139 ↗

FDA Product Code

HSZ

Device Class

Class I

Regulation

21 CFR Part 878.4820

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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  Class I

  FDA 510(k) K905207 Active Cleared 22 Jan 1991

• Fixation Devices and Bone Plate

  Class II

  FDA 510(k) K910175 Active Cleared 21 Jun 1991

• Micro-Aire Model 2060

  Class I

  FDA 510(k) K913369 Active Cleared 1 Nov 1991

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  Class I

  FDA 510(k) K905383 Active Cleared 18 Jun 1991

• Microaire(R) Facial Bone Plating System

  Class II

  FDA 510(k) K914998 Active Cleared 2 Jun 1992

See all devices from Micro Surgical Instruments Corp. →