CEMENT EXTRACTION INSTRUMENT SET— 510(k) K780135

Name: FDA 510(k) clearance K780135
Creator: U.S. Food and Drug Administration
Published: 1978-01-31

Substantially Equivalent

Orthopedic Equipment Co., Inc.

FDA 510(k) clearance K780135 for CEMENT EXTRACTION INSTRUMENT SET, Substantially Equivalent on 1978-01-31. Applicant: Orthopedic Equipment Co., Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Equipment Co., Inc.
Product code: Code KDG
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1978-01-24
Decision date: 1978-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KDG

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K952678 — STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT1995-07-10
K952200 — OMNI-JUG1995-06-29
K894785 — SURGICAL CHISEL/OSTEOTOME1989-08-18
K891471 — SIL-MED WASTE FLUID DUMP BAG1989-08-15
K872947 — POREX QUALITY PLASTIC SURGERY INSTRUMENTS1987-08-21

More clearances from Orthopedic Equipment Co., Inc.

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K834035 — UNIVERSAL SELF-ALIGNING ACETABULAR COM1984-06-19
K841189 — OEC/REZAIAN SPINAL FIXATOR1984-05-16
K800530 — SCHLEIN TRI-SURFACE ANKLE1980-04-02
K781445 — SPREADER1979-09-27
K790209 — FILTER SYSTEM, ALTNER DISPOSABLE1979-02-26

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