Overwatch PCF

Primary DI
00840606191685
Brand
Overwatch PCF
Company
SPINAL ELEMENTS, INC.
Model
33021-000
Device description
PERSUADER, OUTER SLEEVE
Published
2026-07-31
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840606191685PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840606191685008406061916858406061916850840606191685

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic rod reducerA heavy-duty, hand-held manual surgical instrument intended to be used to reduce or seat an implantable rod into the saddle of an implant (i.e., bone screw, spinal hook) used as a component of a system to apply force to a series of vertebrae to correct scoliosis (lateral curvature of the spine) or other spinal conditions. When the rod lies medial or lateral to the implant channel this instrument allows for controlled translation of the rod into the saddle of the screws and/or hooks. The surgeon is able to control the positioning (bending) of the rod into the saddle. Once the rod is securely seated in the saddle it is locked into position with a plug or a setscrew. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
7606070121customerservice@spinalelements.com

Regulatory Flags#

DUNS number
610712213
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840606197007MERCURY61085-003-012026-10-16
00840606197014MERCURY61085-003-022026-10-16
00840606197021MERCURY61085-004-012026-10-16
00840606197038MERCURY61085-004-022026-10-16
00840606104074Hero01001-0012015-07-08
00840606104081Hero01001-0022015-07-08
00840606104098Hero01001-0052015-07-08
00840606104104Hero01001-0102015-07-08
00840606104111Hero01002-0012015-07-08
00840606104128Hero01002-0032015-07-08
00840606104135Hero01002-0082015-07-08
00840606104142Hero01003-0012015-07-08
00840606104159Hero01003-0052015-07-08
00840606104166Hero01003-0102015-07-08
00840606104173Hero01004-0052015-07-08
00840606104180Hero01004-0102015-07-08
00840606191425Primus66580-0012026-09-30
00840606191432Primus66580-0022026-09-30
00840606191449Primus66581-0102026-09-30
00840606191456Primus66581-0122026-09-30

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10840642149838Proficient® Posterior Cervical Spine SystemSpine Wave, Inc.LXH2026-10-20
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