FDA.reportPublic FDA data

SPICCA-SP

Primary DI
06009527234176
Brand
SPICCA-SP
Company
SOUTHERN MEDICAL (PTY) LTD
Model
ACC-O-15-14-04-12
Device description
SPICCA PEEK-TI cage,15x14x04x12
Published
2026-06-09
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
OVEIntervertebral Fusion Device With Integrated Fixation, Cervical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OVEIntervertebral Fusion Device With Integrated Fixation, CervicalOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K230608000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K230608000SPICCA Stand-Alone Cervical Fusion CagesSouthern Medical (Pty) , Ltd.2023-08-14OVE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06009527234176PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06009527234176060095272341766009527234176

GMDN Terms#

Term, Definition table
TermDefinition
Metal-polymer composite spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated device made of a non-bioabsorbable synthetic polymer with a metallic coating that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.

Regulatory Flags#

DUNS number
567466073
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06009527200652SASCASASCA-3-37-092026-04-24
06009527224672CMFCNS-SD-1.5X42026-04-24
06009527224689CMFCNS-SD-1.5X52026-04-24
06009527224696CMFCNS-SD-2.0X52026-04-24
06009527226188CMFCNS-SD-2.0X62026-04-24
06009527226195CMFCNS-SD-1.5X4-G2026-04-24
06009527226201CMFCNS-SD-1.5X6-G2026-04-24
06009527226218CMFCNS-SD-1.5X5-G2026-04-24
06009527229189CMFMDS-ST-1.5X42026-04-24
06009527229196CMFMDS-ST-1.5X62026-04-24
06009527229202CMFMDS-ST-1.5X82026-04-24
06009527229219CMFMDS-ST-1.5X102026-04-24
06009527229226CMFMDS-ST-1.5X122026-04-24
06009527229233CMFMDS-ST-1.5X142026-04-24
06009527229240CMFMDS-ST-1.8X52026-04-24
06009527229257CMFMDS-ST-1.8X72026-04-24
06009527229660CMFCNS-SD-2.0X82026-04-24
06009527229677CMFMDS-ST-2.0X52026-04-24
06009527229684CMFMDS-ST-2.0X62026-04-24
06009527229691CMFMDS-ST-2.0X82026-04-24

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00810017914548Saber-C Body (PT), 14x17x6 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
00810017914555Saber-C Body (PT), 14x17x8 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
00810017914562Saber-C Body (PT), 14x17x7 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
00810017914579Saber-C Body (PT), 14x17x9 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
00810017914586Saber-C Body (PT), 14x17x10 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
00810017914647Saber-C Plate, 14x17x10 12 deg.ELEVATION SPINE, INC.OVE2026-07-23
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