Spine Pro

Primary DI
00848657067287
Brand
Spine Pro
Company
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
Model
2803
Device description
Spine Pro Bayonet Kerrison, 3mm, 230mm, 40 degree
Published
2018-04-26
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
HAERONGEUR, MANUAL

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HAERongeur, ManualNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K023868000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K023868000DAN KERRISON RONGEURS, MODELS K1 + BILLY 1Dannoritzer Medical Instruments2003-02-07HAE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00848657067287PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00848657067287008486570672878486570672870848657067287

GMDN Terms#

Term, Definition table
TermDefinition
Bone punch, reusableA hand-held manual surgical instrument with a cutting/biting action used to cut small cross-sectional pieces of bone typically for biopsy or fixation procedures during a surgical intervention. It is typically designed with a long, thin, two-part sliding shaft (the upper part sliding along the lower part) which is joined to sprung (self-opening), pivoted, pistol grip handles. The working end terminates with a sharp, angled, cutting jaw that closes over an endpiece when the handles are squeezed together cutting through the bone. It is available in various sizes and designs (e.g., it can have upward or downward located jaws) and is made of high-grade stainless steel. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
839138955
Device count
1
Lot or batch
true
Serial number
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00848657078535AEDAED2717B2026-10-20
00848657078542AEDAED2718B2026-10-20
00848657078559AEDAED2719B2026-10-20
00848657078481AED8815SB2026-10-08
00848657078498AED8810SB2026-10-08
00848657078504AED1010122026-10-08
00848657078511AED10121-A2026-10-08
00848657078528AEDAED26173AD2026-10-08
00848657083805AED1010162026-10-08
00848657083904AED1010012026-10-08
00848657078467AED101021-A2026-10-05
00848657078474AED101011-A2026-10-05
00848657083782AED1012112026-10-05
00848657083812AED1013112026-10-05
00848657083843AED1010662026-10-05
00848657083874AED1010002026-10-05
00848657083898AED1010212026-10-05
00848657084956AED101013T2026-10-05
00848657084963AED101066-L2026-10-05
00848657084970AED101066-S2026-10-05

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
B382SD9228132210Surgical DirectSurgical Direct, Inc.HAE2026-10-20
B382SD9228132220Surgical DirectSurgical Direct, Inc.HAE2026-10-20
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