FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OSTEONICS OMNIFIT HA HIP STEM SERIES, OSTEONICS SECUR-FIT HA HIP STEM SERIES, OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS

K Number: K982032 · Decision Jul 9, 1998
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
158
Applicant Total
178
Review Days
29

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
OSTEONICS OMNIFIT HA HIP STEM SERIES, OSTEONICS SECUR-FIT HA HIP STEM SERIES, OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS
K Number
K982032
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonics Corp.
Date Received
June 10, 1998
Decision Date
July 9, 1998
Product Code
MEH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MEH), ordered by most recent decision date.

View all

Other Clearances by Osteonics Corp.

K Number Device Name
K983657 OSTEONICS SERIES 7000 AD TIBIAL TRAY
K980070 OSTEONICS HA-COATED DEVICES
K984375 OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLY
K982798 OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEM
K984585 OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVE
K990203 OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS
K990158 OSTEONICS COMBINATION SCREW RING/BLOCKER
K984302 OSTEONICS SPINAL SYSTEM CYLINDRICAL BONE SCREWS
K984353 OSTEO 9MM IC TIBIAL NAIL
K983502 OSTEONICS SECUR-FIT AD GENERATION II ACETABULAR COMPONENT SYSTEM
Search all 178 clearances from Osteonics Corp. →