FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS
K Number: K870781
·
Decision Mar 9, 1987
Classifications
1
FEI Numbers
223
Registration Numbers
223
Same Product Code
11
Applicant Total
111
Review Days
11
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
- ACROMED WALLIE-HEINIG DISECTOR/ELEVATORS
- K Number
- K870781
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Buckman Co., Inc.
- Date Received
- February 26, 1987
- Decision Date
- March 9, 1987
- Product Code
- GEG
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GEG | Elevator, Surgical, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GEG), ordered by most recent decision date.
ELEVATORS, VARIOUS TYPES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SEPTUM ELEVATOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURGICAL ELEVATOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
LIGATURE NEEDLES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
1.1 TWIST DRILLS AND 1.2 CORTICAL DRILLS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Other Clearances by Buckman Co., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K961320 | CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM | Jun 25, 1998 | Substantially Equivalent |
| K974641 | FUTURELASE 3000/3002 ERBIUM LASER SYSTEM | Jun 8, 1998 | Substantially Equivalent |
| K964252 | ORTHOCHUCK | May 27, 1997 | Substantially Equivalent |
| K950099 | SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM | Jan 16, 1997 | Substantially Equivalent for Some Indications |
| K960451 | WEBB-MORLEY SPINE SYSTEM | Apr 18, 1996 | Substantially Equivalent for Some Indications |
| K950999 | KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS | Jan 25, 1996 | Substantially Equivalent |
| K945756 | IMAGN(TM) 2000 SYSTEM | Dec 19, 1995 | Substantially Equivalent |
| K940003 | VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT | Oct 19, 1995 | Substantially Equivalent |
| K951117 | LIHTAN 532 LASER | Oct 18, 1995 | Substantially Equivalent |
| K942751 | VANGUARD SERIES GAS REGULATORS | Feb 9, 1995 | Substantially Equivalent |