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

MACROSORBOS PROTECTIVE SHEET

K Number: K994158 · Decision Jul 24, 2000
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
1313
Applicant Total
17
Review Days
228

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
MACROSORBOS PROTECTIVE SHEET
K Number
K994158
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Macropore Biosurgery, Inc.
Date Received
December 9, 1999
Decision Date
July 24, 2000
Product Code
HRS
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
HRS Plate, Fixation, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Macropore Biosurgery, Inc.

K Number Device Name
K042261 MACROPORE PURICEL LIPOPLASTY SYSTEM
K041105 MACROPORE HYDROSORB SPINE SYSTEM
K031955 MACROPORE SURGI-WRAP MAST BIORESORBABLE SHEET
K031785 MACROPORE CARDIO-WRAP (TS)
K024169 MACROPORE OS RECONSTRUCTION
K023643 MACROPORE SURGICAL BARRIER FILM
K021164 MACROPORE OS TRAUMA
K012025 MACROPORE SURGIWRAP (TS)
K012769 MACROPORE ENT RECONSTRUCTION FILM
K012413 MACROPORE FX, PS, NS, LP
Search all 17 clearances from Macropore Biosurgery, Inc. →