Atlas FDA

MULTIPLE MANUAL SURGICAL INSTRUMENTS

FDA 510(k) clearance K832686 · decided 1983-10-14

Clearance details

K-number
K832686
Device name
MULTIPLE MANUAL SURGICAL INSTRUMENTS
Applicant
Hirata Sangyo Co. USA, Inc.
Decision
Substantially Equivalent
Date received
1983-08-02
Decision date
1983-10-14
Days to decision
73 days
Clearance type
Traditional
Product code
HTO
Device class
1
Regulation number
888.4540
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Hirata Sangyo Co. USA

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
SYNTHES RIA SYSTEM (EXPANDED INDICATIONS) (K111437)Synthes (USA) Products, LLC2011-08-10
SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONS (K042899)Synthes (Usa)2005-03-16
MODIFICATION TO SYNTHES (USA) REAMER IRRIGATOR ASPIRATOR (RIA) SYSTEM (K013527)Synthes (Usa)2001-12-21
SYNTHES REAMER/IRRIGATOR/ASPIRATOR (RIA) SYSTEM (K993335)Synthes (Usa)2000-06-12
FLEXIBLE INTRAMEDULLARY REAMER (K954915)Zimmer, Inc.1995-12-28
COMBINATION REAMER (K903248)Onyx Medical Corp.1990-07-30
MCCONNELL REAMER GUIDE (K885100)Mcconnell Orthopedic1989-01-13
WARSAW ORTHOPEDIC POINTED REAMER (K870845)Warsaw Orthopedic, Inc.1987-03-11
ABC-1000 SMALL JOINT REAMERS (K862933)Instrumentation Industries, Inc.1986-08-18
MEDULLARY CANAL SCRAPERS (K811081)The Anspach Effort, Inc.1981-04-29
C.C.F. FEMORAL DEBRIDEMENT PROBE (K790996)Depuy, Inc.1979-06-27
FLEXIBLE REAMER, GUIDE WIRE SYSTEM (K790307)3M Company1979-02-22

Recalls involving this device

No recalls on record reference this clearance.