Atlas FDA

CEMENTRIFUGE

FDA 510(k) clearance K851205 · decided 1985-07-16

Clearance details

K-number
K851205
Device name
CEMENTRIFUGE
Applicant
Biodynamic Technologies, Inc.
Decision
Substantially Equivalent
Date received
1985-03-26
Decision date
1985-07-16
Days to decision
112 days
Clearance type
Traditional
Product code
JDZ
Device class
1
Regulation number
888.4210
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Arlington, VA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Biodynamic Technologies

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
EXACTECH ALL POLY ACETABULAR CUP (K934253)Exactech, Inc.1994-04-29
PRISM BONE CEMENT MIXING SYSTEM (K925025)Depuy, Inc.1994-01-05
STRYKER HIGH VACUUM BONE CEMENT MIXER/INJECT SYST (K912190)Stryker Corp.1991-08-29
REUSABLE BOWL AND SPATULA FOR MIXING BONE CEMENTS (K892937)Dentsply Intl.1989-06-22
ZIMMER VACUUM MIXING SYSTEM (K861086)Zimmer, Inc.1986-04-14
MIX EVAC II (K854077)Stryker Corp.1986-01-31
SIMPLEX ENHANCEMENT MIXER (K853310)Howmedica Corp.1985-09-11
ZIMMER BONE CEMENT CENTRIFUGATION SYS (K843219)Zimmer, Inc.1984-11-29
HOWMEDICA MIX-KIT II (K792186)Howmedica Corp.1979-12-05
MIXING BOWL & SPATULA, DISPOSABLE (K780857)Howmedica Corp.1978-06-13
ORTHOMIX (K760636)Diemolding Corp.1976-10-05
MIX EVAC BONE CEMENT (K760617)Stryker Corp.1976-10-05

Recalls involving this device

No recalls on record reference this clearance.